Canonical Allele Identifier: CA1602103251
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221491C= , CM000667.2:g.174221491C= GRCh38
NC_000005.9:g.173648494C= , CM000667.1:g.173648494C= GRCh37
NC_000005.8:g.173581100C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16187C= ENSP00000429863.1:n.*18+16187C=