Canonical Allele Identifier: CA1009656434
Gene: NPHS2 HGNC NCBI

Linked Data

dbSNP Id: rs1674756308

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575962dup , CM000663.2:g.179575962dup GRCh38
NC_000001.10:g.179545097dup , CM000663.1:g.179545097dup GRCh37
NC_000001.9:g.177811720dup NCBI36
NG_007535.1:g.4990dup , LRG_887:g.4990dup

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-96dup XP_005245540.1:n.-96dup
XM_006711529.2:c.-96dup XP_006711592.1:n.-96dup
XM_005245483.3:c.-96dup XP_005245540.1:n.-96dup
XM_017002298.1:c.-96dup XP_016857787.1:n.-96dup
XM_017002299.1:c.-96dup XP_016857788.1:n.-96dup