Canonical Allele Identifier: CA375686178

Gene: ABO

Linked Data

• dbSNP Id: rs1834578065
• MyVariant Identifiers: chr9:g.136131584G>T (hg19) ; chr9:g.133256197G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256197G>T , CM000671.2:g.133256197G>T	GRCh38
NC_000009.11:g.136131584G>T , CM000671.1:g.136131584G>T	GRCh37
NC_000009.10:g.135121405G>T	NCBI36
NG_006669.1:g.21471C>A
NG_006669.2:g.24019C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.563C>A
ENST00000647353.1:n.54-5045C>A
ENST00000651471.1:n.489C>A
ENST00000679909.1:c.28+18965C>A	ENSP00000506089.1:n.28+18965C>A
ENST00000453660.3:n.545C>A
ENST00000538324.2:c.531C>A	ENSP00000483018.1:p.Tyr177Ter
ENST00000611156.4:c.531C>A	ENSP00000483265.1:p.Tyr177Ter
NM_020469.2:c.534C>A	NP_065202.2:p.Tyr178Ter
NM_020469.3:c.534C>A	NP_065202.2:p.Tyr178Ter