Canonical Allele Identifier: CA1898741269
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.29075709C= , CM000672.2:g.29075709C= GRCh38
NC_000010.10:g.29364638C= , CM000672.1:g.29364638C= GRCh37
NC_000010.9:g.29404644C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001747284.1:n.127-3783C=