Canonical Allele Identifier: CA1818149096
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999212T= , CM000670.2:g.126999212T= GRCh38
NC_000008.10:g.128011457T= , CM000670.1:g.128011457T= GRCh37
NC_000008.9:g.128080639T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7343T=