Canonical Allele Identifier: CA296576146

Gene:

Linked Data

• dbSNP Id: rs952434062
• gnomAD v3: 18-10382939-T-A
• gnomAD v4: 18-10382939-T-A
• MyVariant Identifiers: chr18:g.10382936T>A (hg19) ; chr18:g.10382939T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382939T>A , CM000680.2:g.10382939T>A	GRCh38
NC_000018.9:g.10382936T>A , CM000680.1:g.10382936T>A	GRCh37
NC_000018.8:g.10372936T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_935143.1:n.919+1586T>A