Canonical Allele Identifier: CA11521650

Gene: KAT2B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.20042389C>T , CM000665.2:g.20042389C>T	GRCh38
NC_000003.11:g.20083881C>T , CM000665.1:g.20083881C>T	GRCh37
NC_000003.10:g.20058885C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263754.5:c.303+1609C>T MANE Select	ENSP00000263754.4:n.303+1609C>T
ENST00000263754.4:c.303+1609C>T	ENSP00000263754.4:n.303+1609C>T
ENST00000426228.1:n.83+1609C>T
NM_003884.4:c.303+1609C>T	NP_003875.3:n.303+1609C>T
XM_005265528.3:c.303+1609C>T	XP_005265585.1:n.303+1609C>T
XM_011534206.1:c.-193+1609C>T	XP_011532508.1:n.-193+1609C>T
XR_245162.3:n.394+1609C>T
XM_005265528.4:c.303+1609C>T	XP_005265585.1:n.303+1609C>T
XR_001740351.1:n.374+1609C>T
XR_245162.4:n.374+1609C>T
NM_003884.5:c.303+1609C>T MANE Select	NP_003875.3:n.303+1609C>T