Canonical Allele Identifier: CA2137920601
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.54185761C= , CM000676.2:g.54185761C= GRCh38
NC_000014.8:g.54652479C= , CM000676.1:g.54652479C= GRCh37
NC_000014.7:g.53722229C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943882.1:n.360-331G=
XR_943883.1:n.360-331G=
XR_943884.1:n.360-331G=
XR_001750980.1:n.360-331G=
XR_943882.2:n.360-331G=
XR_943883.2:n.360-331G=