Canonical Allele Identifier: CA1818149519
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999544C= , CM000670.2:g.126999544C= GRCh38
NC_000008.10:g.128011789C= , CM000670.1:g.128011789C= GRCh37
NC_000008.9:g.128080971C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7011C=