Canonical Allele Identifier: CA173689895

Gene:

Linked Data

• dbSNP Id: rs750229930
• gnomAD v3: 8-20734937-T-C
• gnomAD v4: 8-20734937-T-C
• MyVariant Identifiers: chr8:g.20592448T>C (hg19) ; chr8:g.20734937T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20734937T>C , CM000670.2:g.20734937T>C	GRCh38
NC_000008.10:g.20592448T>C , CM000670.1:g.20592448T>C	GRCh37
NC_000008.9:g.20636728T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949569.3:n.72-55509T>C