Canonical Allele Identifier: CA2573138767

Gene:

Linked Data

• ClinVar Variation Id: 1525534
• ClinVar RCV Id: RCV002550501
• dbSNP Id: rs2149628912

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707467G>C , CM000667.2:g.112707467G>C	GRCh38
NC_000005.9:g.112043164G>C , CM000667.1:g.112043164G>C	GRCh37
NC_000005.8:g.112071063G>C	NCBI36
NG_008481.4:g.19947G>C , LRG_130:g.19947G>C