Canonical Allele Identifier: CA384023885
Gene: PDE6H HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14978062C>G , CM000674.2:g.14978062C>G GRCh38
NC_000012.11:g.15130996C>G , CM000674.1:g.15130996C>G GRCh37
NC_000012.10:g.15022263C>G NCBI36
NG_016859.1:g.10041C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266395.3:c.50C>G MANE Select ENSP00000266395.2:p.Thr17Ser
ENST00000266395.2:c.50C>G ENSP00000266395.2:p.Thr17Ser
NM_006205.2:c.50C>G NP_006196.1:p.Thr17Ser
XR_931376.1:n.175+11425G>C
XM_017019431.2:c.50C>G XP_016874920.1:p.Thr17Ser
XR_931376.2:n.389+11425G>C
NM_006205.3:c.50C>G MANE Select NP_006196.1:p.Thr17Ser