Canonical Allele Identifier: CA564839882

Gene: NSG2

Linked Data

• dbSNP Id: rs1445076768
• gnomAD v2: 5-173648674-A-C
• gnomAD v3: 5-174221671-A-C
• gnomAD v4: 5-174221671-A-C
• MyVariant Identifiers: chr5:g.173648674A>C (hg19) ; chr5:g.174221671A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221671A>C , CM000667.2:g.174221671A>C	GRCh38
NC_000005.9:g.173648674A>C , CM000667.1:g.173648674A>C	GRCh37
NC_000005.8:g.173581280A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16367A>C	ENSP00000429863.1:n.*18+16367A>C