Canonical Allele Identifier: CA593185753

Gene:

Linked Data

• dbSNP Id: rs1454365948
• gnomAD v2: 10-43813951-A-G
• gnomAD v3: 10-43318503-A-G
• gnomAD v4: 10-43318503-A-G
• MyVariant Identifiers: chr10:g.43813951A>G (hg19) ; chr10:g.43318503A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43318503A>G , CM000672.2:g.43318503A>G	GRCh38
NC_000010.10:g.43813951A>G , CM000672.1:g.43813951A>G	GRCh37
NC_000010.9:g.43133957A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_945902.1:n.16A>G
XR_945902.2:n.106A>G