Canonical Allele Identifier: CA2197752682
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782357A= , CM000677.2:g.95782357A= GRCh38
NC_000015.9:g.96325586A= , CM000677.1:g.96325586A= GRCh37
NC_000015.8:g.94126590A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42832A=