Canonical Allele Identifier: CA2692330522

Gene: ABO

Linked Data

• gnomAD v4: 9-133257303-AGGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257307_133257310del , CM000671.2:g.133257307_133257310del	GRCh38
NC_000009.11:g.136132694_136132697del , CM000671.1:g.136132694_136132697del	GRCh37
NC_000009.10:g.135122515_135122518del	NCBI36
NG_006669.1:g.20361_20364del
NG_006669.2:g.22909_22912del

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.403+102_403+105del
ENST00000647353.1:n.54-6155_54-6152del
ENST00000651471.1:n.329+735_329+738del
ENST00000679909.1:c.28+17855_28+17858del	ENSP00000506089.1:n.28+17855_28+17858del
ENST00000453660.3:n.385+102_385+105del
ENST00000538324.2:c.371+102_371+105del	ENSP00000483018.1:n.371+102_371+105del
ENST00000611156.4:c.371+102_371+105del	ENSP00000483265.1:n.371+102_371+105del
NM_020469.2:c.374+102_374+105del	NP_065202.2:n.374+102_374+105del
NM_020469.3:c.374+102_374+105del	NP_065202.2:n.374+102_374+105del