Canonical Allele Identifier: CA1602103188
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1755679047
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221374A>T , CM000667.2:g.174221374A>T GRCh38
NC_000005.9:g.173648377A>T , CM000667.1:g.173648377A>T GRCh37
NC_000005.8:g.173580983A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16070A>T ENSP00000429863.1:n.*18+16070A>T
Search 100 bp 5'
Search 100 bp 3'