Canonical Allele Identifier: CA1462694203
Gene:

Linked Data

dbSNP Id: rs1756226715

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558085C>T , CM000666.2:g.62558085C>T GRCh38
NC_000004.11:g.63423803C>T , CM000666.1:g.63423803C>T GRCh37
NC_000004.10:g.63106398C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5759C>T