Canonical Allele Identifier: CA807794453

Gene: NSG2

Linked Data

• dbSNP Id: rs1425357503
• MyVariant Identifiers: chr5:g.173648442G>C (hg19) ; chr5:g.174221439G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174221439G>C , CM000667.2:g.174221439G>C	GRCh38
NC_000005.9:g.173648442G>C , CM000667.1:g.173648442G>C	GRCh37
NC_000005.8:g.173581048G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521585.5:c.*18+16135G>C	ENSP00000429863.1:n.*18+16135G>C