Canonical Allele Identifier: CA1009656463

Gene: NPHS2

Linked Data

• dbSNP Id: rs1674756504
• gnomAD v3: 1-179575962-CG-C
• gnomAD v4: 1-179575962-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575967del , CM000663.2:g.179575967del	GRCh38
NC_000001.10:g.179545102del , CM000663.1:g.179545102del	GRCh37
NC_000001.9:g.177811725del	NCBI36
NG_007535.1:g.4987del , LRG_887:g.4987del

Transcript Alleles

HGVS	Amino-acid Change
XM_005245483.2:c.-99del	XP_005245540.1:n.-99del
XM_006711529.2:c.-99del	XP_006711592.1:n.-99del
XM_005245483.3:c.-99del	XP_005245540.1:n.-99del
XM_017002298.1:c.-99del	XP_016857787.1:n.-99del
XM_017002299.1:c.-99del	XP_016857788.1:n.-99del