Canonical Allele Identifier: CA2692330319

Gene: ABO

Linked Data

• gnomAD v4: 9-133255454-GTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255455_133255457del , CM000671.2:g.133255455_133255457del	GRCh38
NC_000009.11:g.136130842_136130844del , CM000671.1:g.136130842_136130844del	GRCh37
NC_000009.10:g.135120663_135120665del	NCBI36
NG_006669.1:g.22211_22213del
NG_006669.2:g.24759_24761del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1303_1305del
ENST00000647353.1:n.54-4305_54-4303del
ENST00000679909.1:c.28+19705_28+19707del	ENSP00000506089.1:n.28+19705_28+19707del
ENST00000453660.3:n.1285_1287del
ENST00000611156.4:c.*209_*211del	ENSP00000483265.1:n.*209_*211del
NM_020469.2:c.*209_*211del	NP_065202.2:n.*209_*211del
NM_020469.3:c.*209_*211del	NP_065202.2:n.*209_*211del