Canonical Allele Identifier: CA1602103326
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221660A= , CM000667.2:g.174221660A= GRCh38
NC_000005.9:g.173648663A= , CM000667.1:g.173648663A= GRCh37
NC_000005.8:g.173581269A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16356A= ENSP00000429863.1:n.*18+16356A=