Canonical Allele Identifier: CA375685836

Gene: ABO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256093T>C , CM000671.2:g.133256093T>C	GRCh38
NC_000009.11:g.136131480T>C , CM000671.1:g.136131480T>C	GRCh37
NC_000009.10:g.135121301T>C	NCBI36
NG_006669.1:g.21575A>G
NG_006669.2:g.24123A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.667A>G
ENST00000647353.1:n.54-4941A>G
ENST00000679909.1:c.28+19069A>G	ENSP00000506089.1:n.28+19069A>G
ENST00000453660.3:n.649A>G
ENST00000538324.2:c.635A>G	ENSP00000483018.1:p.Asp212Gly
ENST00000611156.4:c.635A>G	ENSP00000483265.1:p.Asp212Gly
NM_020469.2:c.638A>G	NP_065202.2:p.Asp213Gly
NM_020469.3:c.638A>G	NP_065202.2:p.Asp213Gly