Canonical Allele Identifier: CA375686304
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256267T>A , CM000671.2:g.133256267T>A GRCh38
NC_000009.11:g.136131654T>A , CM000671.1:g.136131654T>A GRCh37
NC_000009.10:g.135121475T>A NCBI36
NG_006669.1:g.21401A>T
NG_006669.2:g.23949A>T

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.464A>T NP_065202.2:p.Gln155Leu
NM_020469.3:c.464A>T NP_065202.2:p.Gln155Leu
ENST00000453660.3:n.475A>T
ENST00000538324.2:c.461A>T ENSP00000483018.1:p.Gln154Leu
ENST00000611156.4:c.461A>T ENSP00000483265.1:p.Gln154Leu