Canonical Allele Identifier: CA375686327
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256277A>C , CM000671.2:g.133256277A>C GRCh38
NC_000009.11:g.136131664A>C , CM000671.1:g.136131664A>C GRCh37
NC_000009.10:g.135121485A>C NCBI36
NG_006669.1:g.21391T>G
NG_006669.2:g.23939T>G

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.454T>G NP_065202.2:p.Phe152Val
NM_020469.3:c.454T>G NP_065202.2:p.Phe152Val
ENST00000453660.3:n.465T>G
ENST00000538324.2:c.451T>G ENSP00000483018.1:p.Phe151Val
ENST00000611156.4:c.451T>G ENSP00000483265.1:p.Phe151Val