Canonical Allele Identifier: CA1882583327
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834638968

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258260G>A , CM000671.2:g.133258260G>A GRCh38
NC_000009.11:g.136133651G>A , CM000671.1:g.136133651G>A GRCh37
NC_000009.10:g.135123472G>A NCBI36
NG_006669.1:g.19403C>T
NG_006669.2:g.21955C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-128C>T
ENST00000647353.1:n.54-7108C>T
ENST00000651471.1:n.239-128C>T
ENST00000679909.1:c.28+16902C>T ENSP00000506089.1:n.28+16902C>T
ENST00000453660.3:n.216-128C>T
ENST00000538324.2:c.204-128C>T ENSP00000483018.1:n.204-128C>T
ENST00000611156.4:c.204-128C>T ENSP00000483265.1:n.204-128C>T
NM_020469.2:c.204-128C>T NP_065202.2:n.204-128C>T
NM_020469.3:c.204-128C>T NP_065202.2:n.204-128C>T