Canonical Allele Identifier: CA2293960066
Gene:

Linked Data

dbSNP Id: rs1850805816

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756472T>C , CM000680.2:g.31756472T>C GRCh38
NC_000018.9:g.29336435T>C , CM000680.1:g.29336435T>C GRCh37
NC_000018.8:g.27590433T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5667T>C