Canonical Allele Identifier: CA1462694105
Gene:

Linked Data

dbSNP Id: rs1756224554

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557903G>C , CM000666.2:g.62557903G>C GRCh38
NC_000004.11:g.63423621G>C , CM000666.1:g.63423621G>C GRCh37
NC_000004.10:g.63106216G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5941G>C