Canonical Allele Identifier: CA5305888
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs781928216

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257401T>C , CM000671.2:g.133257401T>C GRCh38
NC_000009.11:g.136132788T>C , CM000671.1:g.136132788T>C GRCh37
NC_000009.10:g.135122609T>C NCBI36
NG_006669.1:g.20267A>G
NG_006669.2:g.22815A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+8A>G
ENST00000647353.1:n.54-6249A>G
ENST00000651471.1:n.329+641A>G
ENST00000679909.1:c.28+17761A>G ENSP00000506089.1:n.28+17761A>G
ENST00000453660.3:n.385+8A>G
ENST00000538324.2:c.371+8A>G ENSP00000483018.1:n.371+8A>G
ENST00000611156.4:c.371+8A>G ENSP00000483265.1:n.371+8A>G
NM_020469.2:c.374+8A>G NP_065202.2:n.374+8A>G
NM_020469.3:c.374+8A>G NP_065202.2:n.374+8A>G