Canonical Allele Identifier: CA026385
Gene:

Linked Data

ClinVar Variation Id: 13086
dbSNP Id: rs387906521

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303715G>A , CM000675.2:g.48303715G>A GRCh38
NC_000013.10:g.48877851G>A , CM000675.1:g.48877851G>A GRCh37
NC_000013.9:g.47775852G>A NCBI36
NG_009009.1:g.4969G>A , LRG_517:g.4969G>A