Canonical Allele Identifier: CA1799829983

Gene: CNGB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86647809T= , CM000670.2:g.86647809T=	GRCh38
NC_000008.10:g.87660037T= , CM000670.1:g.87660037T=	GRCh37
NC_000008.9:g.87729153T=	NCBI36
NG_016980.1:g.100867A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000320005.6:c.982A= MANE Select	ENSP00000316605.5:p.Met328=
ENST00000681546.1:n.802A=
ENST00000681746.1:c.982A=	ENSP00000505959.1:p.Met328=
ENST00000320005.5:c.982A=	ENSP00000316605.5:p.Met328=
NM_019098.4:c.982A=	NP_061971.3:p.Met328=
XM_011517138.1:c.568A=	XP_011515440.1:p.Met190=
XM_011517138.2:c.568A=	XP_011515440.1:p.Met190=
NM_019098.5:c.982A= MANE Select	NP_061971.3:p.Met328=