Canonical Allele Identifier: CA2525319866
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260282A>G , CM000671.2:g.133260282A>G GRCh38
NG_006669.1:g.17368T>C
NG_006669.2:g.19933T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.186-416T>C
ENST00000647353.1:n.54-9130T>C
ENST00000651471.1:n.191-416T>C
ENST00000679909.1:c.28+14880T>C ENSP00000506089.1:n.28+14880T>C
ENST00000453660.3:n.168-416T>C
ENST00000538324.2:c.156-416T>C ENSP00000483018.1:n.156-416T>C
ENST00000611156.4:c.156-416T>C ENSP00000483265.1:n.156-416T>C
NM_020469.2:c.156-416T>C NP_065202.2:n.156-416T>C
NM_020469.3:c.156-416T>C NP_065202.2:n.156-416T>C