Canonical Allele Identifier: CA33653600

Gene: NPHS2

Linked Data

• dbSNP Id: rs1046868806
• gnomAD v3: 1-179575465-G-T
• gnomAD v4: 1-179575465-G-T
• MyVariant Identifiers: chr1:g.179544600G>T (hg19) ; chr1:g.179575465G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575465G>T , CM000663.2:g.179575465G>T	GRCh38
NC_000001.10:g.179544600G>T , CM000663.1:g.179544600G>T	GRCh37
NC_000001.9:g.177811223G>T	NCBI36
NG_007535.1:g.5485C>A , LRG_887:g.5485C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.274+126C>A MANE Select	ENSP00000356587.4:n.274+126C>A
ENST00000367615.8:c.274+126C>A	ENSP00000356587.4:n.274+126C>A
ENST00000367616.4:c.274+126C>A	ENSP00000356588.4:n.274+126C>A
NM_001297575.1:c.274+126C>A	NP_001284504.1:n.274+126C>A
NM_014625.3:c.274+126C>A , LRG_887t1:c.274+126C>A	NP_055440.1:n.274+126C>A
XM_005245483.2:c.274+126C>A	XP_005245540.1:n.274+126C>A
XM_006711529.2:c.274+126C>A	XP_006711592.1:n.274+126C>A
XM_005245483.3:c.274+126C>A	XP_005245540.1:n.274+126C>A
XM_017002298.1:c.274+126C>A	XP_016857787.1:n.274+126C>A
XM_017002299.1:c.274+126C>A	XP_016857788.1:n.274+126C>A
NM_001297575.2:c.274+126C>A	NP_001284504.1:n.274+126C>A
NM_014625.4:c.274+126C>A MANE Select	NP_055440.1:n.274+126C>A