Canonical Allele Identifier: CA1168497158
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56262312C= , CM000663.2:g.56262312C= GRCh38
NC_000001.10:g.56727984C= , CM000663.1:g.56727984C= GRCh37
NC_000001.9:g.56500572C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.760-13112G= ENSP00000493138.1:n.760-13112G=
ENST00000641346.1:c.367-13112G=
ENST00000641415.1:c.193-8419G=
ENST00000641494.1:c.379-13112G=
ENST00000642129.1:c.769-13112G=