Canonical Allele Identifier: CA1129725195
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834964053

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274357T>C , CM000671.2:g.133274357T>C GRCh38
NC_000009.11:g.136149773T>C , CM000671.1:g.136149773T>C GRCh37
NC_000009.10:g.135139594T>C NCBI36
NG_006669.1:g.3277A>G
NG_006669.2:g.5858A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+805A>G
ENST00000647353.1:n.53+805A>G
ENST00000651471.1:n.63+1605A>G
ENST00000679909.1:c.28+805A>G ENSP00000506089.1:n.28+805A>G
ENST00000453660.3:n.40+805A>G
ENST00000538324.2:c.28+805A>G ENSP00000483018.1:n.28+805A>G
ENST00000611156.4:c.28+805A>G ENSP00000483265.1:n.28+805A>G
NM_020469.2:c.28+805A>G NP_065202.2:n.28+805A>G
NM_020469.3:c.28+805A>G NP_065202.2:n.28+805A>G