Canonical Allele Identifier: CA132640548
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs555585524

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221507C>G , CM000667.2:g.174221507C>G GRCh38
NC_000005.9:g.173648510C>G , CM000667.1:g.173648510C>G GRCh37
NC_000005.8:g.173581116C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16203C>G ENSP00000429863.1:n.*18+16203C>G