Canonical Allele Identifier: CA2839095961
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258139G>A , CM000671.2:g.133258139G>A GRCh38
NC_000009.11:g.136133529G>A , CM000671.1:g.136133529G>A GRCh37
NC_000009.10:g.135123350G>A NCBI36
NG_006669.1:g.19525C>T
NG_006669.2:g.22076C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-7C>T
ENST00000647353.1:n.54-6987C>T
ENST00000651471.1:n.239-7C>T
ENST00000679909.1:c.28+17023C>T ENSP00000506089.1:n.28+17023C>T
ENST00000453660.3:n.216-7C>T
ENST00000538324.2:c.204-7C>T ENSP00000483018.1:n.204-7C>T
ENST00000611156.4:c.204-7C>T ENSP00000483265.1:n.204-7C>T
NM_020469.2:c.204-7C>T NP_065202.2:n.204-7C>T
NM_020469.3:c.204-7C>T NP_065202.2:n.204-7C>T