Canonical Allele Identifier: CA564839846

Gene: NSG2

Linked Data

• dbSNP Id: rs1212429866
• gnomAD v2: 5-173648311-TG-T
• gnomAD v3: 5-174221308-TG-T
• gnomAD v4: 5-174221308-TG-T
• MyVariant Identifiers: chr5:g.173648312del (hg19) ; chr5:g.174221309del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221311del , CM000667.2:g.174221311del	GRCh38
NC_000005.9:g.173648314del , CM000667.1:g.173648314del	GRCh37
NC_000005.8:g.173580920del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16007del	ENSP00000429863.1:n.*18+16007del