Canonical Allele Identifier: CA377631702
Gene: PDE6C HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.95386436G>T (hg19) chr10:g.93626679G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93626679G>T , CM000672.2:g.93626679G>T GRCh38
NC_000010.10:g.95386436G>T , CM000672.1:g.95386436G>T GRCh37
NC_000010.9:g.95376426G>T NCBI36
NG_016752.1:g.19092G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371447.4:c.979G>T MANE Select ENSP00000360502.3:p.Gly327Ter
ENST00000371447.3:c.979G>T ENSP00000360502.3:p.Gly327Ter
NM_006204.3:c.979G>T NP_006195.3:p.Gly327Ter
NM_006204.4:c.979G>T MANE Select NP_006195.3:p.Gly327Ter
Search 100 bp 5'
Search 100 bp 3'