Canonical Allele Identifier: CA1882580976
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256332G= , CM000671.2:g.133256332G= GRCh38
NC_000009.11:g.136131719G= , CM000671.1:g.136131719G= GRCh37
NC_000009.10:g.135121540G= NCBI36
NG_006669.1:g.21336C=
NG_006669.2:g.23884C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.428C=
ENST00000647353.1:n.54-5180C=
ENST00000651471.1:n.354C=
ENST00000679909.1:c.28+18830C= ENSP00000506089.1:n.28+18830C=
ENST00000453660.3:n.410C=
ENST00000538324.2:c.396C= ENSP00000483018.1:p.Phe132=
ENST00000611156.4:c.396C= ENSP00000483265.1:p.Phe132=
NM_020469.2:c.399C= NP_065202.2:p.Phe133=
NM_020469.3:c.399C= NP_065202.2:p.Phe133=