Canonical Allele Identifier: CA1573442177

Gene:

Linked Data

• ClinVar Variation Id: 1017270
• ClinVar RCV Id: RCV003770675
• dbSNP Id: rs1580995288

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707342T>G , CM000667.2:g.112707342T>G	GRCh38
NC_000005.9:g.112043039T>G , CM000667.1:g.112043039T>G	GRCh37
NC_000005.8:g.112070938T>G	NCBI36
NG_008481.4:g.19822T>G , LRG_130:g.19822T>G