Canonical Allele Identifier: CA2725308619
Gene: PDE6H HGNC NCBI

Linked Data

dbSNP Id: rs1592305649

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14977966T>C , CM000674.2:g.14977966T>C GRCh38
NC_000012.11:g.15130900T>C , CM000674.1:g.15130900T>C GRCh37
NC_000012.10:g.15022167T>C NCBI36
NG_016859.1:g.9945T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000266395.3:c.-41-6T>C MANE Select ENSP00000266395.2:n.-41-6T>C
ENST00000266395.2:c.-41-6T>C ENSP00000266395.2:n.-41-6T>C
NM_006205.2:c.-41-6T>C NP_006196.1:n.-41-6T>C
XR_931376.1:n.175+11521A>G
XM_017019431.2:c.-47T>C XP_016874920.1:n.-47T>C
XR_931376.2:n.389+11521A>G
NM_006205.3:c.-41-6T>C MANE Select NP_006196.1:n.-41-6T>C