Canonical Allele Identifier: CA377631678
Gene: PDE6C HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.95386433C>G (hg19) chr10:g.93626676C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.93626676C>G , CM000672.2:g.93626676C>G GRCh38
NC_000010.10:g.95386433C>G , CM000672.1:g.95386433C>G GRCh37
NC_000010.9:g.95376423C>G NCBI36
NG_016752.1:g.19089C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371447.4:c.976C>G MANE Select ENSP00000360502.3:p.His326Asp
ENST00000371447.3:c.976C>G ENSP00000360502.3:p.His326Asp
NM_006204.3:c.976C>G NP_006195.3:p.His326Asp
NM_006204.4:c.976C>G MANE Select NP_006195.3:p.His326Asp
Search 100 bp 5'
Search 100 bp 3'