Canonical Allele Identifier: CA1818149959
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999809C= , CM000670.2:g.126999809C= GRCh38
NC_000008.10:g.128012054C= , CM000670.1:g.128012054C= GRCh37
NC_000008.9:g.128081236C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6746C=