Canonical Allele Identifier: CA375686318
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256273G>T , CM000671.2:g.133256273G>T GRCh38
NC_000009.11:g.136131660G>T , CM000671.1:g.136131660G>T GRCh37
NC_000009.10:g.135121481G>T NCBI36
NG_006669.1:g.21395C>A
NG_006669.2:g.23943C>A

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.458C>A NP_065202.2:p.Thr153Asn
NM_020469.3:c.458C>A NP_065202.2:p.Thr153Asn
ENST00000453660.3:n.469C>A
ENST00000538324.2:c.455C>A ENSP00000483018.1:p.Thr152Asn
ENST00000611156.4:c.455C>A ENSP00000483265.1:p.Thr152Asn