Canonical Allele Identifier: CA1328680874
Gene: PNKD HGNC NCBI

Linked Data

dbSNP Id: rs1048371804
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218270445C>T , CM000664.2:g.218270445C>T GRCh38
NC_000002.11:g.219135168C>T , CM000664.1:g.219135168C>T GRCh37
NC_000002.10:g.218843412C>T NCBI36
NG_017060.1:g.5054C>T
NG_033036.1:g.4726G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000691799.1:n.70+725C>T
ENST00000248451.7:c.-91C>T ENSP00000248451.3:n.-91C>T
NM_001077399.2:c.-91C>T NP_001070867.1:n.-91C>T
NM_015488.4:c.-91C>T NP_056303.3:n.-91C>T
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