Canonical Allele Identifier: CA1882590602
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834961136

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274211G>A , CM000671.2:g.133274211G>A GRCh38
NC_000009.11:g.136149627G>A , CM000671.1:g.136149627G>A GRCh37
NC_000009.10:g.135139448G>A NCBI36
NG_006669.1:g.3424C>T
NG_006669.2:g.6004C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+951C>T
ENST00000647353.1:n.53+951C>T
ENST00000651471.1:n.63+1751C>T
ENST00000679909.1:c.28+951C>T ENSP00000506089.1:n.28+951C>T
ENST00000453660.3:n.40+951C>T
ENST00000538324.2:c.28+951C>T ENSP00000483018.1:n.28+951C>T
ENST00000611156.4:c.28+951C>T ENSP00000483265.1:n.28+951C>T
NM_020469.2:c.28+951C>T NP_065202.2:n.28+951C>T
NM_020469.3:c.28+951C>T NP_065202.2:n.28+951C>T