Canonical Allele Identifier: CA2197752696
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782375T= , CM000677.2:g.95782375T= GRCh38
NC_000015.9:g.96325604T= , CM000677.1:g.96325604T= GRCh37
NC_000015.8:g.94126608T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42814T=