Canonical Allele Identifier: CA2197752671
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782338G= , CM000677.2:g.95782338G= GRCh38
NC_000015.9:g.96325567G= , CM000677.1:g.96325567G= GRCh37
NC_000015.8:g.94126571G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932654.1:n.148-42851G=