Canonical Allele Identifier: CA2573138731

Gene:

Linked Data

• ClinVar Variation Id: 1369440
• ClinVar RCV Id: RCV003772593
• dbSNP Id: rs2149627912

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707317G>C , CM000667.2:g.112707317G>C	GRCh38
NC_000005.9:g.112043014G>C , CM000667.1:g.112043014G>C	GRCh37
NC_000005.8:g.112070913G>C	NCBI36
NG_008481.4:g.19797G>C , LRG_130:g.19797G>C