Canonical Allele Identifier: CA1898741355
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075782C= , CM000672.2:g.29075782C= GRCh38
NC_000010.10:g.29364711C= , CM000672.1:g.29364711C= GRCh37
NC_000010.9:g.29404717C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001747284.1:n.127-3710C=