Canonical Allele Identifier: CA2649317245
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575984G>A , CM000663.2:g.179575984G>A GRCh38
NC_000001.10:g.179545119G>A , CM000663.1:g.179545119G>A GRCh37
NC_000001.9:g.177811742G>A NCBI36
NG_007535.1:g.4966C>T , LRG_887:g.4966C>T

Transcript Alleles

HGVS Amino-acid Change
XM_017002299.1:c.-120C>T XP_016857788.1:n.-120C>T