Canonical Allele Identifier: CA2298481253

Gene:

Linked Data

• dbSNP Id: rs1910118864
• gnomAD v3: 18-41477697-C-G
• gnomAD v4: 18-41477697-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.41477697C>G , CM000680.2:g.41477697C>G	GRCh38
NC_000018.9:g.39057661C>G , CM000680.1:g.39057661C>G	GRCh37
NC_000018.8:g.37311659C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935409.1:n.86-26437C>G