Canonical Allele Identifier: CA5305820
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs782220700

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256223G>A , CM000671.2:g.133256223G>A GRCh38
NC_000009.11:g.136131610G>A , CM000671.1:g.136131610G>A GRCh37
NC_000009.10:g.135121431G>A NCBI36
NG_006669.1:g.21445C>T
NG_006669.2:g.23993C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.537C>T
ENST00000647353.1:n.54-5071C>T
ENST00000651471.1:n.463C>T
ENST00000679909.1:c.28+18939C>T ENSP00000506089.1:n.28+18939C>T
ENST00000453660.3:n.519C>T
ENST00000538324.2:c.505C>T ENSP00000483018.1:p.Leu169=
ENST00000611156.4:c.505C>T ENSP00000483265.1:p.Leu169=
NM_020469.2:c.508C>T NP_065202.2:p.Leu170=
NM_020469.3:c.508C>T NP_065202.2:p.Leu170=