Canonical Allele Identifier: CA2710513776
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2113100979
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221683C>T , CM000667.2:g.174221683C>T GRCh38
NC_000005.9:g.173648686C>T , CM000667.1:g.173648686C>T GRCh37
NC_000005.8:g.173581292C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16379C>T ENSP00000429863.1:n.*18+16379C>T
Search 100 bp 5'
Search 100 bp 3'