Canonical Allele Identifier: CA2649317241
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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