Canonical Allele Identifier: CA206723608

Gene:

Linked Data

• dbSNP Id: rs141809934
• gnomAD v2: 10-43813958-A-G
• gnomAD v3: 10-43318510-A-G
• gnomAD v4: 10-43318510-A-G
• MyVariant Identifiers: chr10:g.43813958A>G (hg19) ; chr10:g.43318510A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43318510A>G , CM000672.2:g.43318510A>G	GRCh38
NC_000010.10:g.43813958A>G , CM000672.1:g.43813958A>G	GRCh37
NC_000010.9:g.43133964A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945902.1:n.23A>G
XR_945902.2:n.113A>G