Canonical Allele Identifier: CA9389762
Gene: NPHS1 HGNC NCBI

Linked Data

dbSNP Id: rs574866409
ExAC: 19:36322026 G / C
gnomAD v2: 19-36322026-G-C
MyVariant Identifiers: chr19:g.36322026G>C (hg19) chr19:g.35831124G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35831124G>C , CM000681.2:g.35831124G>C GRCh38
NC_000019.9:g.36322026G>C , CM000681.1:g.36322026G>C GRCh37
NC_000019.8:g.41013866G>C NCBI36
NG_013356.2:g.43164C>G , LRG_693:g.43164C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378910.10:c.3410C>G MANE Select ENSP00000368190.4:p.Pro1137Arg
ENST00000353632.6:c.3290C>G ENSP00000343634.5:p.Pro1097Arg
ENST00000378910.9:c.3410C>G ENSP00000368190.4:p.Pro1137Arg
NM_004646.3:c.3410C>G , LRG_693t1:c.3410C>G NP_004637.1:p.Pro1137Arg
NM_004646.4:c.3410C>G MANE Select NP_004637.1:p.Pro1137Arg
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