Canonical Allele Identifier: CA778454217
Gene:

Linked Data

dbSNP Id: rs1354028281

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756669T>C , CM000680.2:g.31756669T>C GRCh38
NC_000018.9:g.29336632T>C , CM000680.1:g.29336632T>C GRCh37
NC_000018.8:g.27590630T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5470T>C