Canonical Allele Identifier: CA1882581915
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256962C= , CM000671.2:g.133256962C= GRCh38
NC_000009.11:g.136132349C= , CM000671.1:g.136132349C= GRCh37
NC_000009.10:g.135122170C= NCBI36
NG_006669.1:g.20706G=
NG_006669.2:g.23254G=

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.403+447G=
ENST00000647353.1:n.54-5810G=
ENST00000651471.1:n.330-606G=
ENST00000679909.1:c.28+18200G= ENSP00000506089.1:n.28+18200G=
ENST00000453660.3:n.385+447G=
ENST00000538324.2:c.371+447G= ENSP00000483018.1:n.371+447G=
ENST00000611156.4:c.371+447G= ENSP00000483265.1:n.371+447G=
NM_020469.2:c.374+447G= NP_065202.2:n.374+447G=
NM_020469.3:c.374+447G= NP_065202.2:n.374+447G=