Canonical Allele Identifier: CA200766003
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs903606132

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257299G>A , CM000671.2:g.133257299G>A GRCh38
NC_000009.11:g.136132686G>A , CM000671.1:g.136132686G>A GRCh37
NC_000009.10:g.135122507G>A NCBI36
NG_006669.1:g.20369C>T
NG_006669.2:g.22917C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+110C>T
ENST00000647353.1:n.54-6147C>T
ENST00000651471.1:n.329+743C>T
ENST00000679909.1:c.28+17863C>T ENSP00000506089.1:n.28+17863C>T
ENST00000453660.3:n.385+110C>T
ENST00000538324.2:c.371+110C>T ENSP00000483018.1:n.371+110C>T
ENST00000611156.4:c.371+110C>T ENSP00000483265.1:n.371+110C>T
NM_020469.2:c.374+110C>T NP_065202.2:n.374+110C>T
NM_020469.3:c.374+110C>T NP_065202.2:n.374+110C>T