Canonical Allele Identifier: CA564839863

Gene: NSG2

Linked Data

• dbSNP Id: rs1217131362
• gnomAD v2: 5-173648392-A-G
• gnomAD v3: 5-174221389-A-G
• gnomAD v4: 5-174221389-A-G
• MyVariant Identifiers: chr5:g.173648392A>G (hg19) ; chr5:g.174221389A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221389A>G , CM000667.2:g.174221389A>G	GRCh38
NC_000005.9:g.173648392A>G , CM000667.1:g.173648392A>G	GRCh37
NC_000005.8:g.173580998A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000521585.5:c.*18+16085A>G	ENSP00000429863.1:n.*18+16085A>G