Canonical Allele Identifier: CA2003780297

Gene:

Linked Data

• ClinVar Variation Id: 1903846
• ClinVar RCV Id: RCV002586665
• dbSNP Id: rs1592207763

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119084594T>G , CM000673.2:g.119084594T>G	GRCh38
NC_000011.9:g.118955304T>G , CM000673.1:g.118955304T>G	GRCh37
NC_000011.8:g.118460514T>G	NCBI36
NG_008093.1:g.4718T>G