Canonical Allele Identifier: CA307787133
Gene: NPHS1 HGNC NCBI

Linked Data

dbSNP Id: rs372900073
gnomAD v4: 19-35848389-A-G
MyVariant Identifiers: chr19:g.36339291A>G (hg19) chr19:g.35848389A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35848389A>G , CM000681.2:g.35848389A>G GRCh38
NC_000019.9:g.36339291A>G , CM000681.1:g.36339291A>G GRCh37
NC_000019.8:g.41031131A>G NCBI36
NG_013356.2:g.25899T>C , LRG_693:g.25899T>C
NG_051206.1:g.1755A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.1179T>C MANE Select ENSP00000368190.4:p.His393=
ENST00000353632.6:c.1179T>C ENSP00000343634.5:p.His393=
ENST00000378910.9:c.1179T>C ENSP00000368190.4:p.His393=
ENST00000592132.1:n.186T>C
NM_004646.3:c.1179T>C , LRG_693t1:c.1179T>C NP_004637.1:p.His393=
NM_004646.4:c.1179T>C MANE Select NP_004637.1:p.His393=
Search 100 bp 5'
Search 100 bp 3'