Canonical Allele Identifier: CA375682213
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1286755031

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255621G>C , CM000671.2:g.133255621G>C GRCh38
NC_000009.11:g.136131008G>C , CM000671.1:g.136131008G>C GRCh37
NC_000009.10:g.135120829G>C NCBI36
NG_006669.1:g.22047C>G
NG_006669.2:g.24595C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1139C>G
ENST00000647353.1:n.54-4469C>G
ENST00000679909.1:c.28+19541C>G ENSP00000506089.1:n.28+19541C>G
ENST00000453660.3:n.1121C>G
ENST00000538324.2:c.1103C>G ENSP00000483018.1:p.Pro368Arg
ENST00000611156.4:c.*45C>G ENSP00000483265.1:n.*45C>G
NM_020469.2:c.*45C>G NP_065202.2:n.*45C>G
NM_020469.3:c.*45C>G NP_065202.2:n.*45C>G