Canonical Allele Identifier: CA5305645
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs782672373

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255669C>T , CM000671.2:g.133255669C>T GRCh38
NC_000009.11:g.136131056C>T , CM000671.1:g.136131056C>T GRCh37
NC_000009.10:g.135120877C>T NCBI36
NG_006669.1:g.21999G>A
NG_006669.2:g.24547G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1091G>A
ENST00000647353.1:n.54-4517G>A
ENST00000679909.1:c.28+19493G>A ENSP00000506089.1:n.28+19493G>A
ENST00000453660.3:n.1073G>A
ENST00000538324.2:c.1055G>A ENSP00000483018.1:p.Arg352His
ENST00000611156.4:c.1059G>A ENSP00000483265.1:p.Pro353=
NM_020469.2:c.1062G>A NP_065202.2:p.Pro354=
NM_020469.3:c.1062G>A NP_065202.2:p.Pro354=