Canonical Allele Identifier: CA1818149942
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999796G= , CM000670.2:g.126999796G= GRCh38
NC_000008.10:g.128012041G= , CM000670.1:g.128012041G= GRCh37
NC_000008.9:g.128081223G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6759G=