Canonical Allele Identifier: CA467780026

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136130701G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255314G>C , CM000671.2:g.133255314G>C	GRCh38
NC_000009.11:g.136130701G>C , CM000671.1:g.136130701G>C	GRCh37
NC_000009.10:g.135120522G>C	NCBI36
NG_006669.1:g.22354C>G
NG_006669.2:g.24902C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1446C>G
ENST00000647353.1:n.54-4162C>G
ENST00000679909.1:c.28+19848C>G	ENSP00000506089.1:n.28+19848C>G
ENST00000453660.3:n.1428C>G
ENST00000611156.4:c.*352C>G	ENSP00000483265.1:n.*352C>G
NM_020469.2:c.*352C>G	NP_065202.2:n.*352C>G
NM_020469.3:c.*352C>G	NP_065202.2:n.*352C>G