Canonical Allele Identifier: CA1210326813
Gene: NPHS2 HGNC NCBI

Linked Data

dbSNP Id: rs1674756220

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575960C>T , CM000663.2:g.179575960C>T GRCh38
NC_000001.10:g.179545095C>T , CM000663.1:g.179545095C>T GRCh37
NC_000001.9:g.177811718C>T NCBI36
NG_007535.1:g.4990G>A , LRG_887:g.4990G>A

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-96G>A XP_005245540.1:n.-96G>A
XM_006711529.2:c.-96G>A XP_006711592.1:n.-96G>A
XM_005245483.3:c.-96G>A XP_005245540.1:n.-96G>A
XM_017002298.1:c.-96G>A XP_016857787.1:n.-96G>A
XM_017002299.1:c.-96G>A XP_016857788.1:n.-96G>A