Canonical Allele Identifier: CA2193585387
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152173C= , CM000677.2:g.87152173C= GRCh38
NC_000015.9:g.87695404C= , CM000677.1:g.87695404C= GRCh37
NC_000015.8:g.85496408C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932582.1:n.167-26054C=
XR_932582.2:n.167-26054C=