Canonical Allele Identifier: CA205143427

Gene:

Linked Data

• dbSNP Id: rs769273834
• gnomAD v2: 10-29364711-C-G
• gnomAD v3: 10-29075782-C-G
• gnomAD v4: 10-29075782-C-G
• MyVariant Identifiers: chr10:g.29364711C>G (hg19) ; chr10:g.29075782C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.29075782C>G , CM000672.2:g.29075782C>G	GRCh38
NC_000010.10:g.29364711C>G , CM000672.1:g.29364711C>G	GRCh37
NC_000010.9:g.29404717C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001747284.1:n.127-3710C>G