Canonical Allele Identifier: CA591309060
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257393C>T , CM000671.2:g.133257393C>T GRCh38
NC_000009.11:g.136132780C>T , CM000671.1:g.136132780C>T GRCh37
NC_000009.10:g.135122601C>T NCBI36
NG_006669.1:g.20275G>A
NG_006669.2:g.22823G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+16G>A
ENST00000647353.1:n.54-6241G>A
ENST00000651471.1:n.329+649G>A
ENST00000679909.1:c.28+17769G>A ENSP00000506089.1:n.28+17769G>A
ENST00000453660.3:n.385+16G>A
ENST00000538324.2:c.371+16G>A ENSP00000483018.1:n.371+16G>A
ENST00000611156.4:c.371+16G>A ENSP00000483265.1:n.371+16G>A
NM_020469.2:c.374+16G>A NP_065202.2:n.374+16G>A
NM_020469.3:c.374+16G>A NP_065202.2:n.374+16G>A