Canonical Allele Identifier: CA233312240
Gene: PDE6H HGNC NCBI

Linked Data

dbSNP Id: rs868831954

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14978067C>T , CM000674.2:g.14978067C>T GRCh38
NC_000012.11:g.15131001C>T , CM000674.1:g.15131001C>T GRCh37
NC_000012.10:g.15022268C>T NCBI36
NG_016859.1:g.10046C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266395.3:c.55C>T MANE Select ENSP00000266395.2:p.Pro19Ser
ENST00000266395.2:c.55C>T ENSP00000266395.2:p.Pro19Ser
NM_006205.2:c.55C>T NP_006196.1:p.Pro19Ser
XR_931376.1:n.175+11420G>A
XM_017019431.2:c.55C>T XP_016874920.1:p.Pro19Ser
XR_931376.2:n.389+11420G>A
NM_006205.3:c.55C>T MANE Select NP_006196.1:p.Pro19Ser