Canonical Allele Identifier: CA2516823238
Gene:

Linked Data

dbSNP Id: rs2107331601

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743550T>C , CM000665.2:g.109743550T>C GRCh38
NC_000003.11:g.109462397T>C , CM000665.1:g.109462397T>C GRCh37
NC_000003.10:g.110945087T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63355T>C