Canonical Allele Identifier: CA375686297
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256264G>C , CM000671.2:g.133256264G>C GRCh38
NC_000009.11:g.136131651G>C , CM000671.1:g.136131651G>C GRCh37
NC_000009.10:g.135121472G>C NCBI36
NG_006669.1:g.21404C>G
NG_006669.2:g.23952C>G

Transcript Alleles

HGVS Amino-acid change
NM_020469.2:c.467C>G NP_065202.2:p.Pro156Arg
NM_020469.3:c.467C>G NP_065202.2:p.Pro156Arg
ENST00000453660.3:n.478C>G
ENST00000538324.2:c.464C>G ENSP00000483018.1:p.Pro155Arg
ENST00000611156.4:c.464C>G ENSP00000483265.1:p.Pro155Arg