Canonical Allele Identifier: CA8083653

Gene: CNGB1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.57957342G>T , CM000678.2:g.57957342G>T	GRCh38
NC_000016.9:g.57991246G>T , CM000678.1:g.57991246G>T	GRCh37
NC_000016.8:g.56548747G>T	NCBI36
NG_016351.1:g.18775C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001297.5:c.873C>A MANE Select	NP_001288.3:p.Thr291=
ENST00000251102.13:c.873C>A MANE Select	ENSP00000251102.8:p.Thr291=
NM_001135639.1:c.873C>A	NP_001129111.1:p.Thr291=
NM_001135639.2:c.873C>A	NP_001129111.1:p.Thr291=
NM_001286130.1:c.855C>A	NP_001273059.1:p.Thr285=
NM_001286130.2:c.855C>A	NP_001273059.1:p.Thr285=
NM_001297.4:c.873C>A	NP_001288.3:p.Thr291=
ENST00000251102.12:c.873C>A	ENSP00000251102.8:p.Thr291=
ENST00000311183.8:c.873C>A	ENSP00000311670.4:p.Thr291=
ENST00000564448.5:c.855C>A	ENSP00000454633.1:p.Thr285=
XM_006721134.2:c.873C>A	XP_006721197.1:p.Thr291=