Canonical Allele Identifier: CA131177568

Gene:

Linked Data

• dbSNP Id: rs533368730
• gnomAD v3: 5-162656611-C-A
• gnomAD v4: 5-162656611-C-A
• MyVariant Identifiers: chr5:g.162083617C>A (hg19) ; chr5:g.162656611C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656611C>A , CM000667.2:g.162656611C>A	GRCh38
NC_000005.9:g.162083617C>A , CM000667.1:g.162083617C>A	GRCh37
NC_000005.8:g.162016195C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3491G>T