Canonical Allele Identifier: CA591309499
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1321358948

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258217T>C , CM000671.2:g.133258217T>C GRCh38
NC_000009.11:g.136133608T>C , CM000671.1:g.136133608T>C GRCh37
NC_000009.10:g.135123429T>C NCBI36
NG_006669.1:g.19446A>G
NG_006669.2:g.21998A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-85A>G
ENST00000647353.1:n.54-7065A>G
ENST00000651471.1:n.239-85A>G
ENST00000679909.1:c.28+16945A>G ENSP00000506089.1:n.28+16945A>G
ENST00000453660.3:n.216-85A>G
ENST00000538324.2:c.204-85A>G ENSP00000483018.1:n.204-85A>G
ENST00000611156.4:c.204-85A>G ENSP00000483265.1:n.204-85A>G
NM_020469.2:c.204-85A>G NP_065202.2:n.204-85A>G
NM_020469.3:c.204-85A>G NP_065202.2:n.204-85A>G