Canonical Allele Identifier: CA2692330322

Gene: ABO

Linked Data

• gnomAD v4: 9-133255474-GTGTGTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255480_133255485del , CM000671.2:g.133255480_133255485del	GRCh38
NC_000009.11:g.136130867_136130872del , CM000671.1:g.136130867_136130872del	GRCh37
NC_000009.10:g.135120688_135120693del	NCBI36
NG_006669.1:g.22188_22193del
NG_006669.2:g.24736_24741del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1280_1285del
ENST00000647353.1:n.54-4328_54-4323del
ENST00000679909.1:c.28+19682_28+19687del	ENSP00000506089.1:n.28+19682_28+19687del
ENST00000453660.3:n.1262_1267del
ENST00000611156.4:c.*186_*191del	ENSP00000483265.1:n.*186_*191del
NM_020469.2:c.*186_*191del	NP_065202.2:n.*186_*191del
NM_020469.3:c.*186_*191del	NP_065202.2:n.*186_*191del