Canonical Allele Identifier: CA1168497117
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56262192T= , CM000663.2:g.56262192T= GRCh38
NC_000001.10:g.56727864T= , CM000663.1:g.56727864T= GRCh37
NC_000001.9:g.56500452T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.760-12992A= ENSP00000493138.1:n.760-12992A=
ENST00000641346.1:c.367-12992A=
ENST00000641415.1:c.193-8299A=
ENST00000641494.1:c.379-12992A=
ENST00000642129.1:c.769-12992A=