Canonical Allele Identifier: CA2769486105
Gene: NSG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221241A>C , CM000667.2:g.174221241A>C GRCh38
NC_000005.9:g.173648244A>C , CM000667.1:g.173648244A>C GRCh37
NC_000005.8:g.173580850A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15937A>C ENSP00000429863.1:n.*18+15937A>C