Canonical Allele Identifier: CA1083723770

Gene:

Linked Data

• dbSNP Id: rs1756515468
• gnomAD v3: 5-162656565-G-T
• gnomAD v4: 5-162656565-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.162656565G>T , CM000667.2:g.162656565G>T	GRCh38
NC_000005.9:g.162083571G>T , CM000667.1:g.162083571G>T	GRCh37
NC_000005.8:g.162016149G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001742958.1:n.418+3537C>A