Canonical Allele Identifier: CA807794309

Gene: NSG2

Linked Data

• dbSNP Id: rs1201814699
• gnomAD v3: 5-174221134-A-G
• gnomAD v4: 5-174221134-A-G
• MyVariant Identifiers: chr5:g.173648137A>G (hg19) ; chr5:g.174221134A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221134A>G , CM000667.2:g.174221134A>G	GRCh38
NC_000005.9:g.173648137A>G , CM000667.1:g.173648137A>G	GRCh37
NC_000005.8:g.173580743A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+15830A>G	ENSP00000429863.1:n.*18+15830A>G