Canonical Allele Identifier: CA70747833

Gene: KAT2B

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.20101114G>A , CM000665.2:g.20101114G>A	GRCh38
NC_000003.11:g.20142606G>A , CM000665.1:g.20142606G>A	GRCh37
NC_000003.10:g.20117610G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263754.5:c.670-173G>A MANE Select	ENSP00000263754.4:n.670-173G>A
ENST00000263754.4:c.670-173G>A	ENSP00000263754.4:n.670-173G>A
NM_003884.4:c.670-173G>A	NP_003875.3:n.670-173G>A
XM_005265528.3:c.670-173G>A	XP_005265585.1:n.670-173G>A
XM_011534206.1:c.379-173G>A	XP_011532508.1:n.379-173G>A
XR_245162.3:n.761-173G>A
XM_005265528.4:c.670-173G>A	XP_005265585.1:n.670-173G>A
XM_017007423.1:c.379-173G>A	XP_016862912.1:n.379-173G>A
XM_017007424.1:c.379-173G>A	XP_016862913.1:n.379-173G>A
XR_001740351.1:n.741-173G>A
XR_245162.4:n.741-173G>A
NM_003884.5:c.670-173G>A MANE Select	NP_003875.3:n.670-173G>A