Canonical Allele Identifier: CA478714695

Gene: PDE6H

Linked Data

• MyVariant Identifiers: chr12:g.15131024C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.14978090C>T , CM000674.2:g.14978090C>T	GRCh38
NC_000012.11:g.15131024C>T , CM000674.1:g.15131024C>T	GRCh37
NC_000012.10:g.15022291C>T	NCBI36
NG_016859.1:g.10069C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266395.3:c.78C>T MANE Select	ENSP00000266395.2:p.Phe26=
ENST00000266395.2:c.78C>T	ENSP00000266395.2:p.Phe26=
NM_006205.2:c.78C>T	NP_006196.1:p.Phe26=
XR_931376.1:n.175+11397G>A
XM_017019431.2:c.78C>T	XP_016874920.1:p.Phe26=
XR_931376.2:n.389+11397G>A
NM_006205.3:c.78C>T MANE Select	NP_006196.1:p.Phe26=