Canonical Allele Identifier: CA2197752683
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782358C= , CM000677.2:g.95782358C= GRCh38
NC_000015.9:g.96325587C= , CM000677.1:g.96325587C= GRCh37
NC_000015.8:g.94126591C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42831C=