Canonical Allele Identifier: CA1602103080
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755677058

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221156T>C , CM000667.2:g.174221156T>C GRCh38
NC_000005.9:g.173648159T>C , CM000667.1:g.173648159T>C GRCh37
NC_000005.8:g.173580765T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15852T>C ENSP00000429863.1:n.*18+15852T>C