Canonical Allele Identifier: CA2293960324
Gene:

Linked Data

dbSNP Id: rs1598548119

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31757066C>T , CM000680.2:g.31757066C>T GRCh38
NC_000018.9:g.29337029C>T , CM000680.1:g.29337029C>T GRCh37
NC_000018.8:g.27591027C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5073C>T