Canonical Allele Identifier: CA2786163479
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261643C>G , CM000671.2:g.133261643C>G GRCh38
NC_000009.11:g.136137046C>G , CM000671.1:g.136137046C>G GRCh37
NC_000009.10:g.135126867C>G NCBI36
NG_006669.1:g.16007G>C
NG_006669.2:g.18572G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.129-269G>C
ENST00000647353.1:n.54-10491G>C
ENST00000651471.1:n.134-269G>C
ENST00000679909.1:c.28+13519G>C ENSP00000506089.1:n.28+13519G>C
ENST00000453660.3:n.111-269G>C
ENST00000538324.2:c.99-269G>C ENSP00000483018.1:n.99-269G>C
ENST00000611156.4:c.99-269G>C ENSP00000483265.1:n.99-269G>C
NM_020469.2:c.99-269G>C NP_065202.2:n.99-269G>C
NM_020469.3:c.99-269G>C NP_065202.2:n.99-269G>C