Canonical Allele Identifier: CA298296842

Gene:

Linked Data

• dbSNP Id: rs763483280
• gnomAD v2: 18-29336478-C-A
• gnomAD v3: 18-31756515-C-A
• gnomAD v4: 18-31756515-C-A
• MyVariant Identifiers: chr18:g.29336478C>A (hg19) ; chr18:g.31756515C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756515C>A , CM000680.2:g.31756515C>A	GRCh38
NC_000018.9:g.29336478C>A , CM000680.1:g.29336478C>A	GRCh37
NC_000018.8:g.27590476C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5624C>A