Canonical Allele Identifier: CA1147571695
Gene: NPHS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575957G= , CM000663.2:g.179575957G= GRCh38
NC_000001.10:g.179545092G= , CM000663.1:g.179545092G= GRCh37
NC_000001.9:g.177811715G= NCBI36
NG_007535.1:g.4993C= , LRG_887:g.4993C=

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-93C= XP_005245540.1:n.-93C=
XM_006711529.2:c.-93C= XP_006711592.1:n.-93C=
XM_005245483.3:c.-93C= XP_005245540.1:n.-93C=
XM_017002298.1:c.-93C= XP_016857787.1:n.-93C=
XM_017002299.1:c.-93C= XP_016857788.1:n.-93C=