Canonical Allele Identifier: CA1009656467
Gene: NPHS2 HGNC NCBI

Linked Data

dbSNP Id: rs1674756641
gnomAD v3: 1-179575967-G-A
gnomAD v4: 1-179575967-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575967G>A , CM000663.2:g.179575967G>A GRCh38
NC_000001.10:g.179545102G>A , CM000663.1:g.179545102G>A GRCh37
NC_000001.9:g.177811725G>A NCBI36
NG_007535.1:g.4983C>T , LRG_887:g.4983C>T

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-103C>T XP_005245540.1:n.-103C>T
XM_006711529.2:c.-103C>T XP_006711592.1:n.-103C>T
XM_005245483.3:c.-103C>T XP_005245540.1:n.-103C>T
XM_017002298.1:c.-103C>T XP_016857787.1:n.-103C>T
XM_017002299.1:c.-103C>T XP_016857788.1:n.-103C>T
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