Canonical Allele Identifier: CA375682194
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1407649047

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255610A>G , CM000671.2:g.133255610A>G GRCh38
NC_000009.11:g.136130997A>G , CM000671.1:g.136130997A>G GRCh37
NC_000009.10:g.135120818A>G NCBI36
NG_006669.1:g.22058T>C
NG_006669.2:g.24606T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1150T>C
ENST00000647353.1:n.54-4458T>C
ENST00000679909.1:c.28+19552T>C ENSP00000506089.1:n.28+19552T>C
ENST00000453660.3:n.1132T>C
ENST00000538324.2:c.1114T>C ENSP00000483018.1:p.Trp372Arg
ENST00000611156.4:c.*56T>C ENSP00000483265.1:n.*56T>C
NM_020469.2:c.*56T>C NP_065202.2:n.*56T>C
NM_020469.3:c.*56T>C NP_065202.2:n.*56T>C