Canonical Allele Identifier: CA209919191
Gene: KAT6B HGNC NCBI

Linked Data

dbSNP Id: rs10466033

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.74943248A>G , CM000672.2:g.74943248A>G GRCh38
NC_000010.10:g.76703006A>G , CM000672.1:g.76703006A>G GRCh37
NC_000010.9:g.76373012A>G NCBI36
NG_032048.1:g.121836A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000287239.10:c.622-16722A>G MANE Select ENSP00000287239.4:p.=
ENST00000372711.2:c.622-16722A>G ENSP00000361796.1:p.=
ENST00000372714.6:c.622-16722A>G ENSP00000361799.1:p.=
ENST00000372724.6:c.622-16722A>G ENSP00000361809.2:p.=
ENST00000372725.6:c.622-16722A>G ENSP00000361810.1:p.=
ENST00000647637.1:c.622-16722A>G ENSP00000497620.1:p.=
ENST00000647642.1:c.622-16722A>G ENSP00000497723.1:p.=
ENST00000647666.1:c.622-16722A>G ENSP00000497307.1:p.=
ENST00000648048.1:c.622-16722A>G ENSP00000497325.1:p.=
ENST00000648159.1:c.622-16722A>G ENSP00000497197.1:p.=
ENST00000648302.1:n.616-16722A>G
ENST00000648369.1:c.622-16722A>G ENSP00000496795.1:p.=
ENST00000648370.1:c.622-16722A>G ENSP00000497804.1:p.=
ENST00000648483.1:c.622-16722A>G ENSP00000498153.1:p.=
ENST00000648725.1:c.622-16722A>G ENSP00000497841.1:p.=
ENST00000648892.1:c.622-16722A>G ENSP00000497048.1:p.=
ENST00000648899.1:c.622-16722A>G ENSP00000497198.1:p.=
ENST00000649006.1:c.622-16722A>G ENSP00000498139.1:p.=
ENST00000649375.1:c.622-16722A>G ENSP00000498141.1:p.=
ENST00000649442.1:c.622-16722A>G ENSP00000498102.1:p.=
ENST00000649463.1:c.622-16722A>G ENSP00000497166.1:p.=
ENST00000649645.1:n.597-16722A>G
ENST00000649657.1:c.622-16722A>G ENSP00000497491.1:p.=
ENST00000650048.1:c.622-16722A>G ENSP00000497813.1:p.=
ENST00000650232.1:c.622-16722A>G ENSP00000497570.1:p.=
ENST00000650330.1:n.1108-16722A>G
ENST00000650380.1:n.1101-16722A>G
ENST00000650517.1:n.860-16722A>G
ENST00000287239.8:c.622-16722A>G ENSP00000287239.4:p.=
ENST00000372711.1:c.622-16722A>G ENSP00000361796.1:p.=
ENST00000372714.5:c.622-16722A>G ENSP00000361799.1:p.=
ENST00000372724.5:c.622-16722A>G ENSP00000361809.1:p.=
ENST00000372725.5:c.622-16722A>G ENSP00000361810.1:p.=
NM_001256468.1:c.622-16722A>G NP_001243397.1:p.=
NM_001256469.1:c.622-16722A>G NP_001243398.1:p.=
NM_012330.3:c.622-16722A>G NP_036462.2:p.=
XM_005269664.2:c.622-16722A>G XP_005269721.1:p.=
XR_246132.2:n.2357-1497A>G
XM_017016000.2:c.622-16722A>G XP_016871489.1:p.=
XM_017016002.1:c.622-16722A>G XP_016871491.1:p.=
XM_017016003.1:c.622-16722A>G XP_016871492.1:p.=
XM_017016004.2:c.622-16722A>G XP_016871493.1:p.=
XM_017016005.2:c.622-16722A>G XP_016871494.1:p.=
XM_017016006.2:c.622-16722A>G XP_016871495.1:p.=
XM_017016008.2:c.622-16722A>G XP_016871497.1:p.=
XM_017016009.1:c.622-16722A>G XP_016871498.1:p.=
NM_012330.4:c.622-16722A>G MANE Select NP_036462.2:p.=
NM_001370132.1:c.622-16722A>G NP_001357061.1:p.=
NM_001370133.1:c.622-16722A>G NP_001357062.1:p.=
NM_001370134.1:c.84-16722A>G NP_001357063.1:p.=
NM_001370135.1:c.84-16722A>G NP_001357064.1:p.=
NM_001370136.1:c.622-16722A>G NP_001357065.1:p.=
NM_001370137.1:c.622-16722A>G NP_001357066.1:p.=
NM_001370138.1:c.622-16722A>G NP_001357067.1:p.=
NM_001370139.1:c.622-16722A>G NP_001357068.1:p.=
NM_001370140.1:c.622-16722A>G NP_001357069.1:p.=
NM_001370141.1:c.622-16722A>G NP_001357070.1:p.=
NM_001370142.1:c.622-16722A>G NP_001357071.1:p.=
NM_001370143.1:c.622-16722A>G NP_001357072.1:p.=
NM_001370144.1:c.622-16722A>G NP_001357073.1:p.=
NM_001256468.2:c.622-16722A>G NP_001243397.1:p.=
NM_001256469.2:c.622-16722A>G NP_001243398.1:p.=