Canonical Allele Identifier: CA200765990
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs995761511

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257261T>G , CM000671.2:g.133257261T>G GRCh38
NC_000009.11:g.136132648T>G , CM000671.1:g.136132648T>G GRCh37
NC_000009.10:g.135122469T>G NCBI36
NG_006669.1:g.20407A>C
NG_006669.2:g.22955A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+148A>C
ENST00000647353.1:n.54-6109A>C
ENST00000651471.1:n.329+781A>C
ENST00000679909.1:c.28+17901A>C ENSP00000506089.1:n.28+17901A>C
ENST00000453660.3:n.385+148A>C
ENST00000538324.2:c.371+148A>C ENSP00000483018.1:n.371+148A>C
ENST00000611156.4:c.371+148A>C ENSP00000483265.1:n.371+148A>C
NM_020469.2:c.374+148A>C NP_065202.2:n.374+148A>C
NM_020469.3:c.374+148A>C NP_065202.2:n.374+148A>C