Canonical Allele Identifier: CA1004589656

Gene:

Linked Data

• dbSNP Id: rs1652357795
• gnomAD v3: 1-94564035-A-G
• gnomAD v4: 1-94564035-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94564035A>G , CM000663.2:g.94564035A>G	GRCh38
NC_000001.10:g.95029591A>G , CM000663.1:g.95029591A>G	GRCh37
NC_000001.9:g.94802179A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001738161.1:n.461+422A>G