Canonical Allele Identifier: CA1139851445
Gene: NPHS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575980G= , CM000663.2:g.179575980G= GRCh38
NC_000001.10:g.179545115G= , CM000663.1:g.179545115G= GRCh37
NC_000001.9:g.177811738G= NCBI36
NG_007535.1:g.4970C= , LRG_887:g.4970C=

Transcript Alleles

HGVS Amino-acid Change
XM_017002298.1:c.-116C= XP_016857787.1:n.-116C=
XM_017002299.1:c.-116C= XP_016857788.1:n.-116C=