Canonical Allele Identifier: CA2649317239
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575980G>T , CM000663.2:g.179575980G>T GRCh38
NC_000001.10:g.179545115G>T , CM000663.1:g.179545115G>T GRCh37
NC_000001.9:g.177811738G>T NCBI36
NG_007535.1:g.4970C>A , LRG_887:g.4970C>A

Transcript Alleles

HGVS Amino-acid Change
XM_017002298.1:c.-116C>A XP_016857787.1:n.-116C>A
XM_017002299.1:c.-116C>A XP_016857788.1:n.-116C>A