Canonical Allele Identifier: CA2001592066
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.114360674T= , CM000673.2:g.114360674T= GRCh38
NC_000011.9:g.114231396T= , CM000673.1:g.114231396T= GRCh37
NC_000011.8:g.113736606T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120567.1:n.3792A=