Canonical Allele Identifier: CA298296848
Gene:

Linked Data

dbSNP Id: rs555978495

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756592T>C , CM000680.2:g.31756592T>C GRCh38
NC_000018.9:g.29336555T>C , CM000680.1:g.29336555T>C GRCh37
NC_000018.8:g.27590553T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5547T>C