Canonical Allele Identifier: CA778454219
Gene:

Linked Data

dbSNP Id: rs1240107345

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756693T>C , CM000680.2:g.31756693T>C GRCh38
NC_000018.9:g.29336656T>C , CM000680.1:g.29336656T>C GRCh37
NC_000018.8:g.27590654T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5446T>C