Canonical Allele Identifier: CA802056771

Gene:

Linked Data

• ClinVar Variation Id: 649909
• ClinVar RCV Id: RCV003768507 ; RCV003947995
• dbSNP Id: rs1461935725
• gnomAD v3: 5-112707332-G-C
• gnomAD v4: 5-112707332-G-C
• MyVariant Identifiers: chr5:g.112043029G>C (hg19) ; chr5:g.112707332G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707332G>C , CM000667.2:g.112707332G>C	GRCh38
NC_000005.9:g.112043029G>C , CM000667.1:g.112043029G>C	GRCh37
NC_000005.8:g.112070928G>C	NCBI36
NG_008481.4:g.19812G>C , LRG_130:g.19812G>C