Canonical Allele Identifier: CA1602103231
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755680035

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221458T>G , CM000667.2:g.174221458T>G GRCh38
NC_000005.9:g.173648461T>G , CM000667.1:g.173648461T>G GRCh37
NC_000005.8:g.173581067T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16154T>G ENSP00000429863.1:n.*18+16154T>G