Canonical Allele Identifier: CA1882580476
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256151C= , CM000671.2:g.133256151C= GRCh38
NC_000009.11:g.136131538C= , CM000671.1:g.136131538C= GRCh37
NC_000009.10:g.135121359C= NCBI36
NG_006669.1:g.21517G=
NG_006669.2:g.24065G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.609G=
ENST00000647353.1:n.54-4999G=
ENST00000651471.1:n.535G=
ENST00000679909.1:c.28+19011G= ENSP00000506089.1:n.28+19011G=
ENST00000453660.3:n.591G=
ENST00000538324.2:c.577G= ENSP00000483018.1:p.Asp193=
ENST00000611156.4:c.577G= ENSP00000483265.1:p.Asp193=
NM_020469.2:c.580G= NP_065202.2:p.Asp194=
NM_020469.3:c.580G= NP_065202.2:p.Asp194=