Canonical Allele Identifier: CA405407951
Gene: NPHS1 HGNC NCBI

Linked Data

gnomAD v4: 19-35849558-T-G
MyVariant Identifiers: chr19:g.36340460T>G (hg19) chr19:g.35849558T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35849558T>G , CM000681.2:g.35849558T>G GRCh38
NC_000019.9:g.36340460T>G , CM000681.1:g.36340460T>G GRCh37
NC_000019.8:g.41032300T>G NCBI36
NG_013356.2:g.24730A>C , LRG_693:g.24730A>C
NG_051206.1:g.2924T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.704A>C MANE Select ENSP00000368190.4:p.Asn235Thr
ENST00000353632.6:c.704A>C ENSP00000343634.5:p.Asn235Thr
ENST00000378910.9:c.704A>C ENSP00000368190.4:p.Asn235Thr
NM_004646.3:c.704A>C , LRG_693t1:c.704A>C NP_004637.1:p.Asn235Thr
NM_004646.4:c.704A>C MANE Select NP_004637.1:p.Asn235Thr
Search 100 bp 5'
Search 100 bp 3'