Canonical Allele Identifier: CA467782945
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131665G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256278G>T , CM000671.2:g.133256278G>T GRCh38
NC_000009.11:g.136131665G>T , CM000671.1:g.136131665G>T GRCh37
NC_000009.10:g.135121486G>T NCBI36
NG_006669.1:g.21390C>A
NG_006669.2:g.23938C>A

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.453C>A NP_065202.2:p.Val151=
NM_020469.3:c.453C>A NP_065202.2:p.Val151=
ENST00000453660.3:n.464C>A
ENST00000538324.2:c.450C>A ENSP00000483018.1:p.Val150=
ENST00000611156.4:c.450C>A ENSP00000483265.1:p.Val150=