Canonical Allele Identifier: CA33654370
Gene: NPHS2 HGNC NCBI

Linked Data

dbSNP Id: rs571045342

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575957G>A , CM000663.2:g.179575957G>A GRCh38
NC_000001.10:g.179545092G>A , CM000663.1:g.179545092G>A GRCh37
NC_000001.9:g.177811715G>A NCBI36
NG_007535.1:g.4993C>T , LRG_887:g.4993C>T

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-93C>T XP_005245540.1:n.-93C>T
XM_006711529.2:c.-93C>T XP_006711592.1:n.-93C>T
XM_005245483.3:c.-93C>T XP_005245540.1:n.-93C>T
XM_017002298.1:c.-93C>T XP_016857787.1:n.-93C>T
XM_017002299.1:c.-93C>T XP_016857788.1:n.-93C>T