Canonical Allele Identifier: CA1083723781
Gene:

Linked Data

dbSNP Id: rs1756515655

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162656579T>C , CM000667.2:g.162656579T>C GRCh38
NC_000005.9:g.162083585T>C , CM000667.1:g.162083585T>C GRCh37
NC_000005.8:g.162016163T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742958.1:n.418+3523A>G