Canonical Allele Identifier: CA2663093398
Gene: PNKD HGNC NCBI

Linked Data

gnomAD v4: 2-218270437-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218270437T>A , CM000664.2:g.218270437T>A GRCh38
NC_000002.11:g.219135160T>A , CM000664.1:g.219135160T>A GRCh37
NC_000002.10:g.218843404T>A NCBI36
NG_017060.1:g.5046T>A
NG_033036.1:g.4734A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691799.1:n.70+717T>A
ENST00000248451.7:c.-99T>A ENSP00000248451.3:n.-99T>A
NM_001077399.2:c.-99T>A NP_001070867.1:n.-99T>A
NM_015488.4:c.-99T>A NP_056303.3:n.-99T>A
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