Canonical Allele Identifier: CA235815
Gene: PDE6C HGNC NCBI

Linked Data

ClinVar Variation Id: 191012
ClinVar RCV Id: RCV000171187
dbSNP Id: rs786205463

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93655770T>C , CM000672.2:g.93655770T>C GRCh38
NC_000010.10:g.95415527T>C , CM000672.1:g.95415527T>C GRCh37
NC_000010.9:g.95405517T>C NCBI36
NG_016752.1:g.48183T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371447.4:c.1946T>C MANE Select ENSP00000360502.3:p.Ile649Thr
ENST00000371447.3:c.1946T>C ENSP00000360502.3:p.Ile649Thr
NM_006204.3:c.1946T>C NP_006195.3:p.Ile649Thr
NM_006204.4:c.1946T>C MANE Select NP_006195.3:p.Ile649Thr