Canonical Allele Identifier: CA1083723808

Gene:

Linked Data

• dbSNP Id: rs1756516267
• gnomAD v3: 5-162656637-A-G
• gnomAD v4: 5-162656637-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656637A>G , CM000667.2:g.162656637A>G	GRCh38
NC_000005.9:g.162083643A>G , CM000667.1:g.162083643A>G	GRCh37
NC_000005.8:g.162016221A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3465T>C