Canonical Allele Identifier: CA026384

Gene:

Linked Data

• ClinVar Variation Id: 13085
• ClinVar RCV Id: RCV000013960
• dbSNP Id: rs387906520
• gnomAD v4: 13-48303724-G-T
• MyVariant Identifiers: chr13:g.48877860G>T (hg19) ; chr13:g.48303724G>T (hg38)
• PubMed: PMID:1881452

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303724G>T , CM000675.2:g.48303724G>T	GRCh38
NC_000013.10:g.48877860G>T , CM000675.1:g.48877860G>T	GRCh37
NC_000013.9:g.47775861G>T	NCBI36
NG_009009.1:g.4978G>T , LRG_517:g.4978G>T