Canonical Allele Identifier: CA2692330333

Gene: ABO

Linked Data

• gnomAD v4: 9-133255515-GGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255523_133255524del , CM000671.2:g.133255523_133255524del	GRCh38
NC_000009.11:g.136130910_136130911del , CM000671.1:g.136130910_136130911del	GRCh37
NC_000009.10:g.135120731_135120732del	NCBI36
NG_006669.1:g.22151_22152del
NG_006669.2:g.24699_24700del

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.1243_1244del
ENST00000647353.1:n.54-4365_54-4364del
ENST00000679909.1:c.28+19645_28+19646del	ENSP00000506089.1:n.28+19645_28+19646del
ENST00000453660.3:n.1225_1226del
ENST00000611156.4:c.*149_*150del	ENSP00000483265.1:n.*149_*150del
NM_020469.2:c.*149_*150del	NP_065202.2:n.*149_*150del
NM_020469.3:c.*149_*150del	NP_065202.2:n.*149_*150del