Canonical Allele Identifier: CA2649317195
Gene: NPHS2 HGNC NCBI

Linked Data

gnomAD v4: 1-179575956-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575956C>T , CM000663.2:g.179575956C>T GRCh38
NC_000001.10:g.179545091C>T , CM000663.1:g.179545091C>T GRCh37
NC_000001.9:g.177811714C>T NCBI36
NG_007535.1:g.4994G>A , LRG_887:g.4994G>A

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-92G>A XP_005245540.1:n.-92G>A
XM_006711529.2:c.-92G>A XP_006711592.1:n.-92G>A
XM_005245483.3:c.-92G>A XP_005245540.1:n.-92G>A
XM_017002298.1:c.-92G>A XP_016857787.1:n.-92G>A
XM_017002299.1:c.-92G>A XP_016857788.1:n.-92G>A
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