Canonical Allele Identifier: CA1129724017
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs500498

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133273232C>A , CM000671.2:g.133273232C>A GRCh38
NG_006669.1:g.4404G>T
NG_006669.2:g.6983G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+1930G>T
ENST00000647353.1:n.53+1930G>T
ENST00000651471.1:n.63+2730G>T
ENST00000679909.1:c.28+1930G>T ENSP00000506089.1:n.28+1930G>T
ENST00000453660.3:n.40+1930G>T
ENST00000538324.2:c.28+1930G>T ENSP00000483018.1:n.28+1930G>T
ENST00000611156.4:c.28+1930G>T ENSP00000483265.1:n.28+1930G>T
NM_020469.2:c.28+1930G>T NP_065202.2:n.28+1930G>T
NM_020469.3:c.28+1930G>T NP_065202.2:n.28+1930G>T