Canonical Allele Identifier: CA778454159

Gene:

Linked Data

• dbSNP Id: rs1462539072
• gnomAD v3: 18-31756489-T-G
• gnomAD v4: 18-31756489-T-G
• MyVariant Identifiers: chr18:g.29336452T>G (hg19) ; chr18:g.31756489T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756489T>G , CM000680.2:g.31756489T>G	GRCh38
NC_000018.9:g.29336452T>G , CM000680.1:g.29336452T>G	GRCh37
NC_000018.8:g.27590450T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5650T>G