Canonical Allele Identifier: CA628433038

Gene:

Linked Data

• dbSNP Id: rs1206718821
• gnomAD v2: 18-10382889-T-G
• gnomAD v3: 18-10382892-T-G
• gnomAD v4: 18-10382892-T-G
• MyVariant Identifiers: chr18:g.10382889T>G (hg19) ; chr18:g.10382892T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.10382892T>G , CM000680.2:g.10382892T>G	GRCh38
NC_000018.9:g.10382889T>G , CM000680.1:g.10382889T>G	GRCh37
NC_000018.8:g.10372889T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935143.1:n.919+1539T>G