Canonical Allele Identifier: CA2710513770
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2113100921

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221616T>C , CM000667.2:g.174221616T>C GRCh38
NC_000005.9:g.173648619T>C , CM000667.1:g.173648619T>C GRCh37
NC_000005.8:g.173581225T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16312T>C ENSP00000429863.1:n.*18+16312T>C