Canonical Allele Identifier: CA371446199

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87588150C>G (hg19) ; chr8:g.86575922C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575922C>G , CM000670.2:g.86575922C>G	GRCh38
NC_000008.10:g.87588150C>G , CM000670.1:g.87588150C>G	GRCh37
NC_000008.9:g.87657266C>G	NCBI36
NG_016980.1:g.172754G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.2312G>C MANE Select	ENSP00000316605.5:p.Arg771Thr
ENST00000681546.1:n.2132G>C
ENST00000681746.1:c.*723G>C	ENSP00000505959.1:n.*723G>C
ENST00000320005.5:c.2312G>C	ENSP00000316605.5:p.Arg771Thr
ENST00000517327.5:c.276+2767G>C	ENSP00000428329.1:n.276+2767G>C
NM_019098.4:c.2312G>C	NP_061971.3:p.Arg771Thr
XM_011517138.1:c.1898G>C	XP_011515440.1:p.Arg633Thr
XM_011517138.2:c.1898G>C	XP_011515440.1:p.Arg633Thr
NM_019098.5:c.2312G>C MANE Select	NP_061971.3:p.Arg771Thr