Canonical Allele Identifier: CA1168497109
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56262177C= , CM000663.2:g.56262177C= GRCh38
NC_000001.10:g.56727849C= , CM000663.1:g.56727849C= GRCh37
NC_000001.9:g.56500437C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.760-12977G= ENSP00000493138.1:n.760-12977G=
ENST00000641346.1:c.367-12977G=
ENST00000641415.1:c.193-8284G=
ENST00000641494.1:c.379-12977G=
ENST00000642129.1:c.769-12977G=