Canonical Allele Identifier: CA1602092060
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174198151T= , CM000667.2:g.174198151T= GRCh38
NC_000005.9:g.173625154T= , CM000667.1:g.173625154T= GRCh37
NC_000005.8:g.173557760T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.214-7049T= ENSP00000429863.1:n.214-7049T=