Canonical Allele Identifier: CA1210326831
Gene: NPHS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575986T= , CM000663.2:g.179575986T= GRCh38
NC_000001.10:g.179545121T= , CM000663.1:g.179545121T= GRCh37
NC_000001.9:g.177811744T= NCBI36
NG_007535.1:g.4964A= , LRG_887:g.4964A=

Transcript Alleles

HGVS Amino-acid Change
XM_017002299.1:c.-122A= XP_016857788.1:n.-122A=