Canonical Allele Identifier: CA849667473

Gene:

Linked Data

• dbSNP Id: rs1382921911
• gnomAD v3: 8-20734916-T-C
• gnomAD v4: 8-20734916-T-C
• MyVariant Identifiers: chr8:g.20592427T>C (hg19) ; chr8:g.20734916T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20734916T>C , CM000670.2:g.20734916T>C	GRCh38
NC_000008.10:g.20592427T>C , CM000670.1:g.20592427T>C	GRCh37
NC_000008.9:g.20636707T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949569.3:n.72-55530T>C