Canonical Allele Identifier: CA2649317240
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575981T>A , CM000663.2:g.179575981T>A GRCh38
NC_000001.10:g.179545116T>A , CM000663.1:g.179545116T>A GRCh37
NC_000001.9:g.177811739T>A NCBI36
NG_007535.1:g.4969A>T , LRG_887:g.4969A>T

Transcript Alleles

HGVS Amino-acid Change
XM_017002298.1:c.-117A>T XP_016857787.1:n.-117A>T
XM_017002299.1:c.-117A>T XP_016857788.1:n.-117A>T