Canonical Allele Identifier: CA1602103197
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221389A= , CM000667.2:g.174221389A= GRCh38
NC_000005.9:g.173648392A= , CM000667.1:g.173648392A= GRCh37
NC_000005.8:g.173580998A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16085A= ENSP00000429863.1:n.*18+16085A=