Canonical Allele Identifier: CA478714577

Gene: PDE6H

Linked Data

• MyVariant Identifiers: chr12:g.15130991T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14978057T>G , CM000674.2:g.14978057T>G	GRCh38
NC_000012.11:g.15130991T>G , CM000674.1:g.15130991T>G	GRCh37
NC_000012.10:g.15022258T>G	NCBI36
NG_016859.1:g.10036T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266395.3:c.45T>G MANE Select	ENSP00000266395.2:p.Gly15=
ENST00000266395.2:c.45T>G	ENSP00000266395.2:p.Gly15=
NM_006205.2:c.45T>G	NP_006196.1:p.Gly15=
XR_931376.1:n.175+11430A>C
XM_017019431.2:c.45T>G	XP_016874920.1:p.Gly15=
XR_931376.2:n.389+11430A>C
NM_006205.3:c.45T>G MANE Select	NP_006196.1:p.Gly15=