Canonical Allele Identifier: CA470795946
Gene: PDE6C HGNC NCBI

Linked Data

gnomAD v4: 10-93626669-C-T
MyVariant Identifiers: chr10:g.95386426C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93626669C>T , CM000672.2:g.93626669C>T GRCh38
NC_000010.10:g.95386426C>T , CM000672.1:g.95386426C>T GRCh37
NC_000010.9:g.95376416C>T NCBI36
NG_016752.1:g.19082C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371447.4:c.969C>T MANE Select ENSP00000360502.3:p.Tyr323=
ENST00000371447.3:c.969C>T ENSP00000360502.3:p.Tyr323=
NM_006204.3:c.969C>T NP_006195.3:p.Tyr323=
NM_006204.4:c.969C>T MANE Select NP_006195.3:p.Tyr323=
Search 100 bp 5'
Search 100 bp 3'