Canonical Allele Identifier: CA2293960316
Gene:

Linked Data

dbSNP Id: rs2031437206

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757058T>C , CM000680.2:g.31757058T>C GRCh38
NC_000018.9:g.29337021T>C , CM000680.1:g.29337021T>C GRCh37
NC_000018.8:g.27591019T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5081T>C