Canonical Allele Identifier: CA1129716083
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834627178

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257641G>A , CM000671.2:g.133257641G>A GRCh38
NC_000009.11:g.136133028G>A , CM000671.1:g.136133028G>A GRCh37
NC_000009.10:g.135122849G>A NCBI36
NG_006669.1:g.20026C>T
NG_006669.2:g.22574C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-99C>T
ENST00000647353.1:n.54-6489C>T
ENST00000651471.1:n.329+401C>T
ENST00000679909.1:c.28+17521C>T ENSP00000506089.1:n.28+17521C>T
ENST00000453660.3:n.252-99C>T
ENST00000538324.2:c.240-99C>T ENSP00000483018.1:n.240-99C>T
ENST00000611156.4:c.240-99C>T ENSP00000483265.1:n.240-99C>T
NM_020469.2:c.240-99C>T NP_065202.2:n.240-99C>T
NM_020469.3:c.240-99C>T NP_065202.2:n.240-99C>T