Canonical Allele Identifier: CA375686497
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256354T>A , CM000671.2:g.133256354T>A GRCh38
NC_000009.11:g.136131741T>A , CM000671.1:g.136131741T>A GRCh37
NC_000009.10:g.135121562T>A NCBI36
NG_006669.1:g.21314A>T
NG_006669.2:g.23862A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.406A>T
ENST00000647353.1:n.54-5202A>T
ENST00000651471.1:n.332A>T
ENST00000679909.1:c.28+18808A>T ENSP00000506089.1:n.28+18808A>T
ENST00000453660.3:n.388A>T
ENST00000538324.2:c.374A>T ENSP00000483018.1:p.Tyr125Phe
ENST00000611156.4:c.374A>T ENSP00000483265.1:p.Tyr125Phe
NM_020469.2:c.377A>T NP_065202.2:p.Tyr126Phe
NM_020469.3:c.377A>T NP_065202.2:p.Tyr126Phe