Canonical Allele Identifier: CA1573442188

Gene:

Linked Data

• ClinVar Variation Id: 1003352
• ClinVar RCV Id: RCV003652131
• dbSNP Id: rs1750550790

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707350C>T , CM000667.2:g.112707350C>T	GRCh38
NC_000005.9:g.112043047C>T , CM000667.1:g.112043047C>T	GRCh37
NC_000005.8:g.112070946C>T	NCBI36
NG_008481.4:g.19830C>T , LRG_130:g.19830C>T