Canonical Allele Identifier: CA467781387

Gene: ABO

Linked Data

• gnomAD v4: 9-133255527-T-C
• MyVariant Identifiers: chr9:g.136130914T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255527T>C , CM000671.2:g.133255527T>C	GRCh38
NC_000009.11:g.136130914T>C , CM000671.1:g.136130914T>C	GRCh37
NC_000009.10:g.135120735T>C	NCBI36
NG_006669.1:g.22141A>G
NG_006669.2:g.24689A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1233A>G
ENST00000647353.1:n.54-4375A>G
ENST00000679909.1:c.28+19635A>G	ENSP00000506089.1:n.28+19635A>G
ENST00000453660.3:n.1215A>G
ENST00000611156.4:c.*139A>G	ENSP00000483265.1:n.*139A>G
NM_020469.2:c.*139A>G	NP_065202.2:n.*139A>G
NM_020469.3:c.*139A>G	NP_065202.2:n.*139A>G