Canonical Allele Identifier: CA915947981

Gene:

Linked Data

• ClinVar Variation Id: 801182
• ClinVar RCV Id: RCV000985734
• dbSNP Id: rs1589891018
• gnomAD v4: 11-5225438-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.5225438T>C , CM000673.2:g.5225438T>C	GRCh38
NC_000011.9:g.5246668T>C , CM000673.1:g.5246668T>C	GRCh37
NC_000011.8:g.5203244T>C	NCBI36
NG_000007.3:g.72178A>G
NG_059281.1:g.6634A>G