Canonical Allele Identifier: CA298296890

Gene:

Linked Data

• dbSNP Id: rs553387308
• gnomAD v3: 18-31756972-A-C
• gnomAD v4: 18-31756972-A-C
• MyVariant Identifiers: chr18:g.29336935A>C (hg19) ; chr18:g.31756972A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.31756972A>C , CM000680.2:g.31756972A>C	GRCh38
NC_000018.9:g.29336935A>C , CM000680.1:g.29336935A>C	GRCh37
NC_000018.8:g.27590933A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_935338.1:n.66-5167A>C