Canonical Allele Identifier: CA1882580489
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256154T= , CM000671.2:g.133256154T= GRCh38
NC_000009.11:g.136131541T= , CM000671.1:g.136131541T= GRCh37
NC_000009.10:g.135121362T= NCBI36
NG_006669.1:g.21514A=
NG_006669.2:g.24062A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.606A=
ENST00000647353.1:n.54-5002A=
ENST00000651471.1:n.532A=
ENST00000679909.1:c.28+19008A= ENSP00000506089.1:n.28+19008A=
ENST00000453660.3:n.588A=
ENST00000538324.2:c.574A= ENSP00000483018.1:p.Ser192=
ENST00000611156.4:c.574A= ENSP00000483265.1:p.Ser192=
NM_020469.2:c.577A= NP_065202.2:p.Ser193=
NM_020469.3:c.577A= NP_065202.2:p.Ser193=