Canonical Allele Identifier: CA1666175695

Gene: PDE7B PDE7B-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136046867C= , CM000668.2:g.136046867C=	GRCh38
NC_000006.11:g.136368005C= , CM000668.1:g.136368005C=	GRCh37
NC_000006.10:g.136409698C=	NCBI36
NG_011994.1:g.200172C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308191.11:c.83-61864C= (PDE7B) MANE Select	ENSP00000310661.6:n.83-61864C=
ENST00000308191.10:c.83-61864C= (PDE7B)	ENSP00000310661.6:n.83-61864C=
ENST00000615259.4:c.238+8339C= (PDE7B)	ENSP00000482117.1:n.238+8339C=
NM_018945.3:c.83-61864C= (PDE7B)	NP_061818.1:n.83-61864C=
XM_005266931.2:c.238+8339C= (PDE7B)	XP_005266988.1:n.238+8339C=
XM_011535755.1:c.200-61864C= (PDE7B)	XP_011534057.1:n.200-61864C=
XR_943018.1:n.2452G= (PDE7B-AS1)
XR_943022.1:n.1998+442G= (PDE7B-AS1)
XR_943025.1:n.2001+442G= (PDE7B-AS1)
XR_943026.1:n.1822-1934G= (PDE7B-AS1)
XR_943029.1:n.1564-1934G= (PDE7B-AS1)
XR_943030.1:n.1563+23357G= (PDE7B-AS1)
NR_149042.1:n.489-1934G= (PDE7B-AS1)
NM_018945.4:c.83-61864C= (PDE7B) MANE Select	NP_061818.1:n.83-61864C=