Canonical Allele Identifier: CA2649317187
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575953del , CM000663.2:g.179575953del GRCh38
NC_000001.10:g.179545088del , CM000663.1:g.179545088del GRCh37
NC_000001.9:g.177811711del NCBI36
NG_007535.1:g.4997del , LRG_887:g.4997del

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-89del XP_005245540.1:n.-89del
XM_006711529.2:c.-89del XP_006711592.1:n.-89del
XM_005245483.3:c.-89del XP_005245540.1:n.-89del
XM_017002298.1:c.-89del XP_016857787.1:n.-89del
XM_017002299.1:c.-89del XP_016857788.1:n.-89del