Canonical Allele Identifier: CA375685102

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131323G>C (hg19) ; chr9:g.133255936G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255936G>C , CM000671.2:g.133255936G>C	GRCh38
NC_000009.11:g.136131323G>C , CM000671.1:g.136131323G>C	GRCh37
NC_000009.10:g.135121144G>C	NCBI36
NG_006669.1:g.21732C>G
NG_006669.2:g.24280C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.824C>G
ENST00000647353.1:n.54-4784C>G
ENST00000679909.1:c.28+19226C>G	ENSP00000506089.1:n.28+19226C>G
ENST00000453660.3:n.806C>G
ENST00000538324.2:c.792C>G	ENSP00000483018.1:p.Tyr264Ter
ENST00000611156.4:c.792C>G	ENSP00000483265.1:p.Tyr264Ter
NM_020469.2:c.795C>G	NP_065202.2:p.Tyr265Ter
NM_020469.3:c.795C>G	NP_065202.2:p.Tyr265Ter