Canonical Allele Identifier: CA806711219

Gene:

Linked Data

• dbSNP Id: rs1175227402
• MyVariant Identifiers: chr5:g.162083527T>G (hg19) ; chr5:g.162656521T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656521T>G , CM000667.2:g.162656521T>G	GRCh38
NC_000005.9:g.162083527T>G , CM000667.1:g.162083527T>G	GRCh37
NC_000005.8:g.162016105T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3581A>C