Canonical Allele Identifier: CA1349715714

Gene: KAT2B

Genomic Alleles

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

Transcript Alleles

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