Canonical Allele Identifier: CA1356887157
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.34921346T= , CM000665.2:g.34921346T= GRCh38
NC_000003.11:g.34962838T= , CM000665.1:g.34962838T= GRCh37
NC_000003.10:g.34937842T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110817.1:n.207-41880A=