Canonical Allele Identifier: CA1210326824
Gene: NPHS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575979C= , CM000663.2:g.179575979C= GRCh38
NC_000001.10:g.179545114C= , CM000663.1:g.179545114C= GRCh37
NC_000001.9:g.177811737C= NCBI36
NG_007535.1:g.4971G= , LRG_887:g.4971G=

Transcript Alleles

HGVS Amino-acid Change
XM_017002298.1:c.-115G= XP_016857787.1:n.-115G=
XM_017002299.1:c.-115G= XP_016857788.1:n.-115G=