Canonical Allele Identifier: CA1899263551
Gene:

Linked Data

dbSNP Id: rs1839591333

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30201874A>C , CM000672.2:g.30201874A>C GRCh38
NC_000010.10:g.30490803A>C , CM000672.1:g.30490803A>C GRCh37
NC_000010.9:g.30530809A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930791.1:n.1193-1613A>C
XR_930791.2:n.1449-1613A>C