Canonical Allele Identifier: CA1920266040

Gene: KAT6B

Linked Data

• dbSNP Id: rs1849834241

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.74943318A>C , CM000672.2:g.74943318A>C	GRCh38
NC_000010.10:g.76703076A>C , CM000672.1:g.76703076A>C	GRCh37
NC_000010.9:g.76373082A>C	NCBI36
NG_032048.1:g.121906A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000287239.10:c.622-16652A>C MANE Select	ENSP00000287239.4:n.622-16652A>C
ENST00000372711.2:c.622-16652A>C	ENSP00000361796.1:n.622-16652A>C
ENST00000372714.6:c.622-16652A>C	ENSP00000361799.1:n.622-16652A>C
ENST00000372724.6:c.622-16652A>C	ENSP00000361809.2:n.622-16652A>C
ENST00000372725.6:c.622-16652A>C	ENSP00000361810.1:n.622-16652A>C
ENST00000647637.1:c.622-16652A>C	ENSP00000497620.1:n.622-16652A>C
ENST00000647642.1:c.622-16652A>C	ENSP00000497723.1:n.622-16652A>C
ENST00000647666.1:c.622-16652A>C	ENSP00000497307.1:n.622-16652A>C
ENST00000648048.1:c.622-16652A>C	ENSP00000497325.1:n.622-16652A>C
ENST00000648159.1:c.622-16652A>C	ENSP00000497197.1:n.622-16652A>C
ENST00000648302.1:n.616-16652A>C
ENST00000648369.1:c.622-16652A>C	ENSP00000496795.1:n.622-16652A>C
ENST00000648370.1:c.622-16652A>C	ENSP00000497804.1:n.622-16652A>C
ENST00000648483.1:c.622-16652A>C	ENSP00000498153.1:n.622-16652A>C
ENST00000648725.1:c.622-16652A>C	ENSP00000497841.1:n.622-16652A>C
ENST00000648892.1:c.622-16652A>C	ENSP00000497048.1:n.622-16652A>C
ENST00000648899.1:c.622-16652A>C	ENSP00000497198.1:n.622-16652A>C
ENST00000649006.1:c.622-16652A>C	ENSP00000498139.1:n.622-16652A>C
ENST00000649375.1:c.622-16652A>C	ENSP00000498141.1:n.622-16652A>C
ENST00000649442.1:c.622-16652A>C	ENSP00000498102.1:n.622-16652A>C
ENST00000649463.1:c.622-16652A>C	ENSP00000497166.1:n.622-16652A>C
ENST00000649645.1:n.597-16652A>C
ENST00000649657.1:c.622-16652A>C	ENSP00000497491.1:n.622-16652A>C
ENST00000650048.1:c.622-16652A>C	ENSP00000497813.1:n.622-16652A>C
ENST00000650232.1:c.622-16652A>C	ENSP00000497570.1:n.622-16652A>C
ENST00000650330.1:n.1108-16652A>C
ENST00000650380.1:n.1101-16652A>C
ENST00000650517.1:n.860-16652A>C
ENST00000287239.8:c.622-16652A>C	ENSP00000287239.4:n.622-16652A>C
ENST00000372711.1:c.622-16652A>C	ENSP00000361796.1:n.622-16652A>C
ENST00000372714.5:c.622-16652A>C	ENSP00000361799.1:n.622-16652A>C
ENST00000372724.5:c.622-16652A>C	ENSP00000361809.1:n.622-16652A>C
ENST00000372725.5:c.622-16652A>C	ENSP00000361810.1:n.622-16652A>C
NM_001256468.1:c.622-16652A>C	NP_001243397.1:n.622-16652A>C
NM_001256469.1:c.622-16652A>C	NP_001243398.1:n.622-16652A>C
NM_012330.3:c.622-16652A>C	NP_036462.2:n.622-16652A>C
XM_005269664.2:c.622-16652A>C	XP_005269721.1:n.622-16652A>C
XR_246132.2:n.2357-1427A>C
XM_017016000.2:c.622-16652A>C	XP_016871489.1:n.622-16652A>C
XM_017016002.1:c.622-16652A>C	XP_016871491.1:n.622-16652A>C
XM_017016003.1:c.622-16652A>C	XP_016871492.1:n.622-16652A>C
XM_017016004.2:c.622-16652A>C	XP_016871493.1:n.622-16652A>C
XM_017016005.2:c.622-16652A>C	XP_016871494.1:n.622-16652A>C
XM_017016006.2:c.622-16652A>C	XP_016871495.1:n.622-16652A>C
XM_017016008.2:c.622-16652A>C	XP_016871497.1:n.622-16652A>C
XM_017016009.1:c.622-16652A>C	XP_016871498.1:n.622-16652A>C
NM_012330.4:c.622-16652A>C MANE Select	NP_036462.2:n.622-16652A>C
NM_001370132.1:c.622-16652A>C	NP_001357061.1:n.622-16652A>C
NM_001370133.1:c.622-16652A>C	NP_001357062.1:n.622-16652A>C
NM_001370134.1:c.84-16652A>C	NP_001357063.1:n.84-16652A>C
NM_001370135.1:c.84-16652A>C	NP_001357064.1:n.84-16652A>C
NM_001370136.1:c.622-16652A>C	NP_001357065.1:n.622-16652A>C
NM_001370137.1:c.622-16652A>C	NP_001357066.1:n.622-16652A>C
NM_001370138.1:c.622-16652A>C	NP_001357067.1:n.622-16652A>C
NM_001370139.1:c.622-16652A>C	NP_001357068.1:n.622-16652A>C
NM_001370140.1:c.622-16652A>C	NP_001357069.1:n.622-16652A>C
NM_001370141.1:c.622-16652A>C	NP_001357070.1:n.622-16652A>C
NM_001370142.1:c.622-16652A>C	NP_001357071.1:n.622-16652A>C
NM_001370143.1:c.622-16652A>C	NP_001357072.1:n.622-16652A>C
NM_001370144.1:c.622-16652A>C	NP_001357073.1:n.622-16652A>C
NM_001256468.2:c.622-16652A>C	NP_001243397.1:n.622-16652A>C
NM_001256469.2:c.622-16652A>C	NP_001243398.1:n.622-16652A>C