Canonical Allele Identifier: CA1328680891
Gene: PNKD HGNC NCBI

Linked Data

dbSNP Id: rs1237458527

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218270464A>C , CM000664.2:g.218270464A>C GRCh38
NC_000002.11:g.219135187A>C , CM000664.1:g.219135187A>C GRCh37
NC_000002.10:g.218843431A>C NCBI36
NG_017060.1:g.5073A>C
NG_033036.1:g.4707T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000691799.1:n.70+744A>C
ENST00000248451.7:c.-72A>C ENSP00000248451.3:n.-72A>C
NM_001077399.2:c.-72A>C NP_001070867.1:n.-72A>C
NM_015488.4:c.-72A>C NP_056303.3:n.-72A>C