Canonical Allele Identifier: CA2786163121
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256373C>G , CM000671.2:g.133256373C>G GRCh38
NC_000009.11:g.136131760C>G , CM000671.1:g.136131760C>G GRCh37
NC_000009.10:g.135121581C>G NCBI36
NG_006669.1:g.21295G>C
NG_006669.2:g.23843G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-17G>C
ENST00000647353.1:n.54-5221G>C
ENST00000651471.1:n.330-17G>C
ENST00000679909.1:c.28+18789G>C ENSP00000506089.1:n.28+18789G>C
ENST00000453660.3:n.386-17G>C
ENST00000538324.2:c.372-17G>C ENSP00000483018.1:n.372-17G>C
ENST00000611156.4:c.372-17G>C ENSP00000483265.1:n.372-17G>C
NM_020469.2:c.375-17G>C NP_065202.2:n.375-17G>C
NM_020469.3:c.375-17G>C NP_065202.2:n.375-17G>C