Canonical Allele Identifier: CA2293960292
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757001C= , CM000680.2:g.31757001C= GRCh38
NC_000018.9:g.29336964C= , CM000680.1:g.29336964C= GRCh37
NC_000018.8:g.27590962C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5138C=