Canonical Allele Identifier: CA807794447
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs1373726049
MyVariant Identifiers: chr5:g.173648424T>G (hg19) chr5:g.174221421T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221421T>G , CM000667.2:g.174221421T>G GRCh38
NC_000005.9:g.173648424T>G , CM000667.1:g.173648424T>G GRCh37
NC_000005.8:g.173581030T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000521585.5:c.*18+16117T>G ENSP00000429863.1:n.*18+16117T>G
Search 100 bp 5'
Search 100 bp 3'