Canonical Allele Identifier: CA1168497137
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56262249G= , CM000663.2:g.56262249G= GRCh38
NC_000001.10:g.56727921G= , CM000663.1:g.56727921G= GRCh37
NC_000001.9:g.56500509G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641109.1:c.760-13049C= ENSP00000493138.1:n.760-13049C=
ENST00000641346.1:c.367-13049C=
ENST00000641415.1:c.193-8356C=
ENST00000641494.1:c.379-13049C=
ENST00000642129.1:c.769-13049C=