Canonical Allele Identifier: CA421998725

Gene: NPHS2

Linked Data

• ClinVar Variation Id: 2863743
• ClinVar RCV Id: RCV003702429
• dbSNP Id: rs1674747331
• gnomAD v4: 1-179575823-C-T
• MyVariant Identifiers: chr1:g.179544958C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575823C>T , CM000663.2:g.179575823C>T	GRCh38
NC_000001.10:g.179544958C>T , CM000663.1:g.179544958C>T	GRCh37
NC_000001.9:g.177811581C>T	NCBI36
NG_007535.1:g.5127G>A , LRG_887:g.5127G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.42G>A MANE Select	ENSP00000356587.4:p.Gly14=
ENST00000367615.8:c.42G>A	ENSP00000356587.4:p.Gly14=
ENST00000367616.4:c.42G>A	ENSP00000356588.4:p.Gly14=
NM_001297575.1:c.42G>A	NP_001284504.1:p.Gly14=
NM_014625.3:c.42G>A , LRG_887t1:c.42G>A	NP_055440.1:p.Gly14=
XM_005245483.2:c.42G>A	XP_005245540.1:p.Gly14=
XM_006711529.2:c.42G>A	XP_006711592.1:p.Gly14=
XM_005245483.3:c.42G>A	XP_005245540.1:p.Gly14=
XM_017002298.1:c.42G>A	XP_016857787.1:p.Gly14=
XM_017002299.1:c.42G>A	XP_016857788.1:p.Gly14=
NM_001297575.2:c.42G>A	NP_001284504.1:p.Gly14=
NM_014625.4:c.42G>A MANE Select	NP_055440.1:p.Gly14=