Canonical Allele Identifier: CA806711268

Gene:

Linked Data

• dbSNP Id: rs1353137056
• MyVariant Identifiers: chr5:g.162083596A>G (hg19) ; chr5:g.162656590A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656590A>G , CM000667.2:g.162656590A>G	GRCh38
NC_000005.9:g.162083596A>G , CM000667.1:g.162083596A>G	GRCh37
NC_000005.8:g.162016174A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3512T>C