Canonical Allele Identifier: CA1799868924

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86633122T= , CM000670.2:g.86633122T=	GRCh38
NC_000008.10:g.87645350T= , CM000670.1:g.87645350T=	GRCh37
NC_000008.9:g.87714466T=	NCBI36
NG_016980.1:g.115554A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1179-229A= MANE Select	ENSP00000316605.5:n.1179-229A=
ENST00000681546.1:n.999-229A=
ENST00000681746.1:c.1179-229A=	ENSP00000505959.1:n.1179-229A=
ENST00000320005.5:c.1179-229A=	ENSP00000316605.5:n.1179-229A=
NM_019098.4:c.1179-229A=	NP_061971.3:n.1179-229A=
XM_011517138.1:c.765-229A=	XP_011515440.1:n.765-229A=
XM_011517138.2:c.765-229A=	XP_011515440.1:n.765-229A=
NM_019098.5:c.1179-229A= MANE Select	NP_061971.3:n.1179-229A=