Canonical Allele Identifier: CA205143429

Gene:

Linked Data

• dbSNP Id: rs947485052
• gnomAD v2: 10-29364723-G-A
• gnomAD v3: 10-29075794-G-A
• gnomAD v4: 10-29075794-G-A
• MyVariant Identifiers: chr10:g.29364723G>A (hg19) ; chr10:g.29075794G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.29075794G>A , CM000672.2:g.29075794G>A	GRCh38
NC_000010.10:g.29364723G>A , CM000672.1:g.29364723G>A	GRCh37
NC_000010.9:g.29404729G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001747284.1:n.127-3698G>A