Canonical Allele Identifier: CA2649317235
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575979del , CM000663.2:g.179575979del GRCh38
NC_000001.10:g.179545114del , CM000663.1:g.179545114del GRCh37
NC_000001.9:g.177811737del NCBI36
NG_007535.1:g.4972del , LRG_887:g.4972del

Transcript Alleles

HGVS Amino-acid Change
XM_017002298.1:c.-114del XP_016857787.1:n.-114del
XM_017002299.1:c.-114del XP_016857788.1:n.-114del