Canonical Allele Identifier: CA2649317212
Gene: NPHS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179575968A>G , CM000663.2:g.179575968A>G GRCh38
NC_000001.10:g.179545103A>G , CM000663.1:g.179545103A>G GRCh37
NC_000001.9:g.177811726A>G NCBI36
NG_007535.1:g.4982T>C , LRG_887:g.4982T>C

Transcript Alleles

HGVS Amino-acid Change
XM_005245483.2:c.-104T>C XP_005245540.1:n.-104T>C
XM_006711529.2:c.-104T>C XP_006711592.1:n.-104T>C
XM_005245483.3:c.-104T>C XP_005245540.1:n.-104T>C
XM_017002298.1:c.-104T>C XP_016857787.1:n.-104T>C
XM_017002299.1:c.-104T>C XP_016857788.1:n.-104T>C