Canonical Allele Identifier: CA1328680865
Gene: PNKD HGNC NCBI

Linked Data

dbSNP Id: rs1690780414

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218270428G>A , CM000664.2:g.218270428G>A GRCh38
NC_000002.11:g.219135151G>A , CM000664.1:g.219135151G>A GRCh37
NC_000002.10:g.218843395G>A NCBI36
NG_017060.1:g.5037G>A
NG_033036.1:g.4743C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000691799.1:n.70+708G>A
ENST00000248451.7:c.-108G>A ENSP00000248451.3:n.-108G>A
NM_001077399.2:c.-108G>A NP_001070867.1:n.-108G>A
NM_015488.4:c.-108G>A NP_056303.3:n.-108G>A