Canonical Allele Identifier: CA2197752660
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782320A= , CM000677.2:g.95782320A= GRCh38
NC_000015.9:g.96325549A= , CM000677.1:g.96325549A= GRCh37
NC_000015.8:g.94126553A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42869A=