Canonical Allele Identifier: CA1210326823
Gene: NPHS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575973A= , CM000663.2:g.179575973A= GRCh38
NC_000001.10:g.179545108A= , CM000663.1:g.179545108A= GRCh37
NC_000001.9:g.177811731A= NCBI36
NG_007535.1:g.4977T= , LRG_887:g.4977T=

Transcript Alleles

HGVS Amino-acid Change
XM_006711529.2:c.-109T= XP_006711592.1:n.-109T=
XM_005245483.3:c.-109T= XP_005245540.1:n.-109T=
XM_017002298.1:c.-109T= XP_016857787.1:n.-109T=
XM_017002299.1:c.-109T= XP_016857788.1:n.-109T=