Canonical Allele Identifier: CA205143431

Gene:

Linked Data

• dbSNP Id: rs1045574502
• gnomAD v2: 10-29364738-T-G
• gnomAD v3: 10-29075809-T-G
• gnomAD v4: 10-29075809-T-G
• MyVariant Identifiers: chr10:g.29364738T>G (hg19) ; chr10:g.29075809T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.29075809T>G , CM000672.2:g.29075809T>G	GRCh38
NC_000010.10:g.29364738T>G , CM000672.1:g.29364738T>G	GRCh37
NC_000010.9:g.29404744T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001747284.1:n.127-3683T>G