Canonical Allele Identifier: CA11438219

Gene: KAT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.20067054C>T , CM000665.2:g.20067054C>T	GRCh38
NC_000003.11:g.20108546C>T , CM000665.1:g.20108546C>T	GRCh37
NC_000003.10:g.20083550C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263754.5:c.304-5279C>T MANE Select	ENSP00000263754.4:n.304-5279C>T
ENST00000263754.4:c.304-5279C>T	ENSP00000263754.4:n.304-5279C>T
ENST00000426228.1:n.84-5279C>T
NM_003884.4:c.304-5279C>T	NP_003875.3:n.304-5279C>T
XM_005265528.3:c.304-5279C>T	XP_005265585.1:n.304-5279C>T
XM_011534206.1:c.-192-4310C>T	XP_011532508.1:n.-192-4310C>T
XR_245162.3:n.395-5279C>T
XM_005265528.4:c.304-5279C>T	XP_005265585.1:n.304-5279C>T
XR_001740351.1:n.375-5279C>T
XR_245162.4:n.375-5279C>T
NM_003884.5:c.304-5279C>T MANE Select	NP_003875.3:n.304-5279C>T