Canonical Allele Identifier: CA33699884

Gene: NPHS2

Linked Data

• dbSNP Id: rs557196708
• gnomAD v3: 1-179559928-A-G
• gnomAD v4: 1-179559928-A-G
• MyVariant Identifiers: chr1:g.179529063A>G (hg19) ; chr1:g.179559928A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179559928A>G , CM000663.2:g.179559928A>G	GRCh38
NC_000001.10:g.179529063A>G , CM000663.1:g.179529063A>G	GRCh37
NC_000001.9:g.177795686A>G	NCBI36
NG_007535.1:g.21022T>C , LRG_887:g.21022T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367615.9:c.452-167T>C MANE Select	ENSP00000356587.4:n.452-167T>C
ENST00000367615.8:c.452-167T>C	ENSP00000356587.4:n.452-167T>C
ENST00000367616.4:c.452-167T>C	ENSP00000356588.4:n.452-167T>C
NM_001297575.1:c.452-167T>C	NP_001284504.1:n.452-167T>C
NM_014625.3:c.452-167T>C , LRG_887t1:c.452-167T>C	NP_055440.1:n.452-167T>C
XM_005245483.2:c.275-167T>C	XP_005245540.1:n.275-167T>C
XM_006711529.2:c.452-167T>C	XP_006711592.1:n.452-167T>C
XM_005245483.3:c.275-167T>C	XP_005245540.1:n.275-167T>C
XM_017002298.1:c.379-167T>C	XP_016857787.1:n.379-167T>C
XM_017002299.1:c.452-167T>C	XP_016857788.1:n.452-167T>C
NM_001297575.2:c.452-167T>C	NP_001284504.1:n.452-167T>C
NM_014625.4:c.452-167T>C MANE Select	NP_055440.1:n.452-167T>C