Canonical Allele Identifier: CA1898741371
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075798C= , CM000672.2:g.29075798C= GRCh38
NC_000010.10:g.29364727C= , CM000672.1:g.29364727C= GRCh37
NC_000010.9:g.29404733C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3694C=