Canonical Allele Identifier: CA1882585041
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133261667T= , CM000671.2:g.133261667T= GRCh38
NC_000009.11:g.136137070T= , CM000671.1:g.136137070T= GRCh37
NC_000009.10:g.135126891T= NCBI36
NG_006669.1:g.15983A=
NG_006669.2:g.18548A=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.129-293A=
ENST00000647353.1:n.54-10515A=
ENST00000651471.1:n.134-293A=
ENST00000679909.1:c.28+13495A= ENSP00000506089.1:n.28+13495A=
ENST00000453660.3:n.111-293A=
ENST00000538324.2:c.99-293A= ENSP00000483018.1:n.99-293A=
ENST00000611156.4:c.99-293A= ENSP00000483265.1:n.99-293A=
NM_020469.2:c.99-293A= NP_065202.2:n.99-293A=
NM_020469.3:c.99-293A= NP_065202.2:n.99-293A=