Canonical Allele Identifier: CA33654374
Gene: NPHS2 HGNC NCBI

Linked Data

dbSNP Id: rs994799587

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575973A>C , CM000663.2:g.179575973A>C GRCh38
NC_000001.10:g.179545108A>C , CM000663.1:g.179545108A>C GRCh37
NC_000001.9:g.177811731A>C NCBI36
NG_007535.1:g.4977T>G , LRG_887:g.4977T>G

Transcript Alleles

HGVS Amino-acid Change
XM_006711529.2:c.-109T>G XP_006711592.1:n.-109T>G
XM_005245483.3:c.-109T>G XP_005245540.1:n.-109T>G
XM_017002298.1:c.-109T>G XP_016857787.1:n.-109T>G
XM_017002299.1:c.-109T>G XP_016857788.1:n.-109T>G