Canonical Allele Identifier: CA2705977144
Gene:

Linked Data

dbSNP Id: rs2109569350

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558216T>C , CM000666.2:g.62558216T>C GRCh38
NC_000004.11:g.63423934T>C , CM000666.1:g.63423934T>C GRCh37
NC_000004.10:g.63106529T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5628T>C