Canonical Allele Identifier: CA200765992
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs868687579

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257265G>A , CM000671.2:g.133257265G>A GRCh38
NC_000009.11:g.136132652G>A , CM000671.1:g.136132652G>A GRCh37
NC_000009.10:g.135122473G>A NCBI36
NG_006669.1:g.20403C>T
NG_006669.2:g.22951C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+144C>T
ENST00000647353.1:n.54-6113C>T
ENST00000651471.1:n.329+777C>T
ENST00000679909.1:c.28+17897C>T ENSP00000506089.1:n.28+17897C>T
ENST00000453660.3:n.385+144C>T
ENST00000538324.2:c.371+144C>T ENSP00000483018.1:n.371+144C>T
ENST00000611156.4:c.371+144C>T ENSP00000483265.1:n.371+144C>T
NM_020469.2:c.374+144C>T NP_065202.2:n.374+144C>T
NM_020469.3:c.374+144C>T NP_065202.2:n.374+144C>T