Canonical Allele Identifier: CA807794535

Gene: NSG2

Linked Data

• dbSNP Id: rs10476102
• MyVariant Identifiers: chr5:g.173648583A>T (hg19) ; chr5:g.174221580A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221580A>T , CM000667.2:g.174221580A>T	GRCh38
NC_000005.9:g.173648583A>T , CM000667.1:g.173648583A>T	GRCh37
NC_000005.8:g.173581189A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16276A>T	ENSP00000429863.1:n.*18+16276A>T