Canonical Allele Identifier: CA2293960149
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756665T= , CM000680.2:g.31756665T= GRCh38
NC_000018.9:g.29336628T= , CM000680.1:g.29336628T= GRCh37
NC_000018.8:g.27590626T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5474T=