Canonical Allele Identifier: CA2580582332
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133257647G>C , CM000671.2:g.133257647G>C GRCh38
NC_000009.11:g.136133034G>C , CM000671.1:g.136133034G>C GRCh37
NC_000009.10:g.135122855G>C NCBI36
NG_006669.1:g.20020C>G
NG_006669.2:g.22568C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.270-105C>G
ENST00000647353.1:n.54-6495C>G
ENST00000651471.1:n.329+395C>G
ENST00000679909.1:c.28+17515C>G ENSP00000506089.1:n.28+17515C>G
ENST00000453660.3:n.252-105C>G
ENST00000538324.2:c.240-105C>G ENSP00000483018.1:n.240-105C>G
ENST00000611156.4:c.240-105C>G ENSP00000483265.1:n.240-105C>G
NM_020469.2:c.240-105C>G NP_065202.2:n.240-105C>G
NM_020469.3:c.240-105C>G NP_065202.2:n.240-105C>G