Canonical Allele Identifier: CA2649317211
Gene: NPHS2 HGNC NCBI

Linked Data

gnomAD v4: 1-179575968-A-C
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Genomic Alleles

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

Transcript Alleles

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