Canonical Allele Identifier: CA778454182
Gene:

Linked Data

dbSNP Id: rs1196686141

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756545T>C , CM000680.2:g.31756545T>C GRCh38
NC_000018.9:g.29336508T>C , CM000680.1:g.29336508T>C GRCh37
NC_000018.8:g.27590506T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5594T>C