Canonical Allele Identifier: CA2649317229
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575976G>T , CM000663.2:g.179575976G>T GRCh38
NC_000001.10:g.179545111G>T , CM000663.1:g.179545111G>T GRCh37
NC_000001.9:g.177811734G>T NCBI36
NG_007535.1:g.4974C>A , LRG_887:g.4974C>A

Transcript Alleles

HGVS Amino-acid Change
XM_006711529.2:c.-112C>A XP_006711592.1:n.-112C>A
XM_017002298.1:c.-112C>A XP_016857787.1:n.-112C>A
XM_017002299.1:c.-112C>A XP_016857788.1:n.-112C>A