Canonical Allele Identifier: CA1882581109
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256389C= , CM000671.2:g.133256389C= GRCh38
NC_000009.11:g.136131776C= , CM000671.1:g.136131776C= GRCh37
NC_000009.10:g.135121597C= NCBI36
NG_006669.1:g.21279G=
NG_006669.2:g.23827G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-33G=
ENST00000647353.1:n.54-5237G=
ENST00000651471.1:n.330-33G=
ENST00000679909.1:c.28+18773G= ENSP00000506089.1:n.28+18773G=
ENST00000453660.3:n.386-33G=
ENST00000538324.2:c.372-33G= ENSP00000483018.1:n.372-33G=
ENST00000611156.4:c.372-33G= ENSP00000483265.1:n.372-33G=
NM_020469.2:c.375-33G= NP_065202.2:n.375-33G=
NM_020469.3:c.375-33G= NP_065202.2:n.375-33G=