Canonical Allele Identifier: CA375682258

Gene: ABO

Linked Data

• dbSNP Id: rs1834557041
• MyVariant Identifiers: chr9:g.136131033C>T (hg19) ; chr9:g.133255646C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255646C>T , CM000671.2:g.133255646C>T	GRCh38
NC_000009.11:g.136131033C>T , CM000671.1:g.136131033C>T	GRCh37
NC_000009.10:g.135120854C>T	NCBI36
NG_006669.1:g.22022G>A
NG_006669.2:g.24570G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1114G>A
ENST00000647353.1:n.54-4494G>A
ENST00000679909.1:c.28+19516G>A	ENSP00000506089.1:n.28+19516G>A
ENST00000453660.3:n.1096G>A
ENST00000538324.2:c.1078G>A	ENSP00000483018.1:p.Gly360Arg
ENST00000611156.4:c.*20G>A	ENSP00000483265.1:n.*20G>A
NM_020469.2:c.*20G>A	NP_065202.2:n.*20G>A
NM_020469.3:c.*20G>A	NP_065202.2:n.*20G>A