Canonical Allele Identifier: CA507085322
Gene: NPHS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1135592
ClinVar RCV Id: RCV001470912
dbSNP Id: rs2146827509
MyVariant Identifiers: chr19:g.36339906C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35849004C>T , CM000681.2:g.35849004C>T GRCh38
NC_000019.9:g.36339906C>T , CM000681.1:g.36339906C>T GRCh37
NC_000019.8:g.41031746C>T NCBI36
NG_013356.2:g.25284G>A , LRG_693:g.25284G>A
NG_051206.1:g.2370C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.984G>A MANE Select ENSP00000368190.4:p.Gln328=
ENST00000353632.6:c.984G>A ENSP00000343634.5:p.Gln328=
ENST00000378910.9:c.984G>A ENSP00000368190.4:p.Gln328=
NM_004646.3:c.984G>A , LRG_693t1:c.984G>A NP_004637.1:p.Gln328=
NM_004646.4:c.984G>A MANE Select NP_004637.1:p.Gln328=
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