Canonical Allele Identifier: CA2710513774
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2113100938

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221642A>C , CM000667.2:g.174221642A>C GRCh38
NC_000005.9:g.173648645A>C , CM000667.1:g.173648645A>C GRCh37
NC_000005.8:g.173581251A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+16338A>C ENSP00000429863.1:n.*18+16338A>C