Canonical Allele Identifier: CA2521547515
Gene: KAT2B HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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