Canonical Allele Identifier: CA205143428

Gene:

Linked Data

• dbSNP Id: rs140875359
• gnomAD v2: 10-29364714-C-G
• gnomAD v3: 10-29075785-C-G
• gnomAD v4: 10-29075785-C-G
• MyVariant Identifiers: chr10:g.29364714C>G (hg19) ; chr10:g.29075785C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.29075785C>G , CM000672.2:g.29075785C>G	GRCh38
NC_000010.10:g.29364714C>G , CM000672.1:g.29364714C>G	GRCh37
NC_000010.9:g.29404720C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001747284.1:n.127-3707C>G