Canonical Allele Identifier: CA132640518

Gene: NSG2

Linked Data

• dbSNP Id: rs533552841
• MyVariant Identifiers: chr5:g.173648249A>T (hg19) ; chr5:g.174221246A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221246A>T , CM000667.2:g.174221246A>T	GRCh38
NC_000005.9:g.173648249A>T , CM000667.1:g.173648249A>T	GRCh37
NC_000005.8:g.173580855A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+15942A>T	ENSP00000429863.1:n.*18+15942A>T