Canonical Allele Identifier: CA2197752688
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782365G= , CM000677.2:g.95782365G= GRCh38
NC_000015.9:g.96325594G= , CM000677.1:g.96325594G= GRCh37
NC_000015.8:g.94126598G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42824G=