Canonical Allele Identifier: CA2696849
Gene:

Linked Data

ClinVar Variation Id: 1337291
ClinVar RCV Id: RCV001820305
dbSNP Id: rs368238225

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765134C>T , CM000665.2:g.169765134C>T GRCh38
NC_000003.11:g.169482922C>T , CM000665.1:g.169482922C>T GRCh37
NC_000003.10:g.170965616C>T NCBI36
NG_016363.1:g.4927G>A , LRG_347:g.4927G>A