Canonical Allele Identifier: CA467782939
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131662G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256275G>A , CM000671.2:g.133256275G>A GRCh38
NC_000009.11:g.136131662G>A , CM000671.1:g.136131662G>A GRCh37
NC_000009.10:g.135121483G>A NCBI36
NG_006669.1:g.21393C>T
NG_006669.2:g.23941C>T

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.456C>T NP_065202.2:p.Phe152=
NM_020469.3:c.456C>T NP_065202.2:p.Phe152=
ENST00000453660.3:n.467C>T
ENST00000538324.2:c.453C>T ENSP00000483018.1:p.Phe151=
ENST00000611156.4:c.453C>T ENSP00000483265.1:p.Phe151=