Canonical Allele Identifier: CA1882590622
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834962051

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133274247G>C , CM000671.2:g.133274247G>C GRCh38
NC_000009.11:g.136149663G>C , CM000671.1:g.136149663G>C GRCh37
NC_000009.10:g.135139484G>C NCBI36
NG_006669.1:g.3388C>G
NG_006669.2:g.5968C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.58+915C>G
ENST00000647353.1:n.53+915C>G
ENST00000651471.1:n.63+1715C>G
ENST00000679909.1:c.28+915C>G ENSP00000506089.1:n.28+915C>G
ENST00000453660.3:n.40+915C>G
ENST00000538324.2:c.28+915C>G ENSP00000483018.1:n.28+915C>G
ENST00000611156.4:c.28+915C>G ENSP00000483265.1:n.28+915C>G
NM_020469.2:c.28+915C>G NP_065202.2:n.28+915C>G
NM_020469.3:c.28+915C>G NP_065202.2:n.28+915C>G