Canonical Allele Identifier: CA1818149092
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999209C= , CM000670.2:g.126999209C= GRCh38
NC_000008.10:g.128011454C= , CM000670.1:g.128011454C= GRCh37
NC_000008.9:g.128080636C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7346C=