Canonical Allele Identifier: CA778454141

Gene:

Linked Data

• dbSNP Id: rs1297666696
• gnomAD v3: 18-31756443-C-T
• gnomAD v4: 18-31756443-C-T
• MyVariant Identifiers: chr18:g.29336406C>T (hg19) ; chr18:g.31756443C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756443C>T , CM000680.2:g.31756443C>T	GRCh38
NC_000018.9:g.29336406C>T , CM000680.1:g.29336406C>T	GRCh37
NC_000018.8:g.27590404C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5696C>T