Canonical Allele Identifier: CA1210326825
Gene: NPHS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575982C= , CM000663.2:g.179575982C= GRCh38
NC_000001.10:g.179545117C= , CM000663.1:g.179545117C= GRCh37
NC_000001.9:g.177811740C= NCBI36
NG_007535.1:g.4968G= , LRG_887:g.4968G=

Transcript Alleles

HGVS Amino-acid Change
XM_017002298.1:c.-118G= XP_016857787.1:n.-118G=
XM_017002299.1:c.-118G= XP_016857788.1:n.-118G=