Canonical Allele Identifier: CA807794435

Gene: NSG2

Linked Data

• dbSNP Id: rs1246051747
• gnomAD v3: 5-174221386-G-A
• gnomAD v4: 5-174221386-G-A
• MyVariant Identifiers: chr5:g.173648389G>A (hg19) ; chr5:g.174221386G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221386G>A , CM000667.2:g.174221386G>A	GRCh38
NC_000005.9:g.173648389G>A , CM000667.1:g.173648389G>A	GRCh37
NC_000005.8:g.173580995G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16082G>A	ENSP00000429863.1:n.*18+16082G>A