Canonical Allele Identifier: CA98367531
Gene:

Linked Data

dbSNP Id: rs981124409

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558007T>C , CM000666.2:g.62558007T>C GRCh38
NC_000004.11:g.63423725T>C , CM000666.1:g.63423725T>C GRCh37
NC_000004.10:g.63106320T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5837T>C