Canonical Allele Identifier: CA2497340478
Gene: PDE6H HGNC NCBI

Linked Data

dbSNP Id: rs1864620585

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14977955dup , CM000674.2:g.14977955dup GRCh38
NC_000012.11:g.15130889dup , CM000674.1:g.15130889dup GRCh37
NC_000012.10:g.15022156dup NCBI36
NG_016859.1:g.9934dup

Transcript Alleles

HGVS Amino-acid change
ENST00000266395.3:c.-41-17dup MANE Select ENSP00000266395.2:n.-41-17dup
ENST00000266395.2:c.-41-17dup ENSP00000266395.2:n.-41-17dup
NM_006205.2:c.-41-17dup NP_006196.1:n.-41-17dup
XR_931376.1:n.175+11532dup
XM_017019431.2:c.-58dup XP_016874920.1:n.-58dup
XR_931376.2:n.389+11532dup
NM_006205.3:c.-41-17dup MANE Select NP_006196.1:n.-41-17dup