Canonical Allele Identifier: CA1602103170
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1581293585

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221358A>G , CM000667.2:g.174221358A>G GRCh38
NC_000005.9:g.173648361A>G , CM000667.1:g.173648361A>G GRCh37
NC_000005.8:g.173580967A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16054A>G ENSP00000429863.1:n.*18+16054A>G