Canonical Allele Identifier: CA344464
Gene:

Linked Data

ClinVar Variation Id: 41400
ClinVar RCV Id: RCV000034302
dbSNP Id: rs199422256

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.169765160G>C , CM000665.2:g.169765160G>C GRCh38
NC_000003.11:g.169482948G>C , CM000665.1:g.169482948G>C GRCh37
NC_000003.10:g.170965642G>C NCBI36
NG_016363.1:g.4901C>G , LRG_347:g.4901C>G