Canonical Allele Identifier: CA2805337965
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782359C>T , CM000677.2:g.95782359C>T GRCh38
NC_000015.9:g.96325588C>T , CM000677.1:g.96325588C>T GRCh37
NC_000015.8:g.94126592C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42830C>T