Canonical Allele Identifier: CA1799868932

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86633132A= , CM000670.2:g.86633132A=	GRCh38
NC_000008.10:g.87645360A= , CM000670.1:g.87645360A=	GRCh37
NC_000008.9:g.87714476A=	NCBI36
NG_016980.1:g.115544T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1179-239T= MANE Select	ENSP00000316605.5:n.1179-239T=
ENST00000681546.1:n.999-239T=
ENST00000681746.1:c.1179-239T=	ENSP00000505959.1:n.1179-239T=
ENST00000320005.5:c.1179-239T=	ENSP00000316605.5:n.1179-239T=
NM_019098.4:c.1179-239T=	NP_061971.3:n.1179-239T=
XM_011517138.1:c.765-239T=	XP_011515440.1:n.765-239T=
XM_011517138.2:c.765-239T=	XP_011515440.1:n.765-239T=
NM_019098.5:c.1179-239T= MANE Select	NP_061971.3:n.1179-239T=