Canonical Allele Identifier: CA180341065

Gene: CNGB3

Linked Data

• dbSNP Id: rs965330046
• MyVariant Identifiers: chr8:g.87645306A>G (hg19) ; chr8:g.86633078A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86633078A>G , CM000670.2:g.86633078A>G	GRCh38
NC_000008.10:g.87645306A>G , CM000670.1:g.87645306A>G	GRCh37
NC_000008.9:g.87714422A>G	NCBI36
NG_016980.1:g.115598T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1179-185T>C MANE Select	ENSP00000316605.5:n.1179-185T>C
ENST00000681546.1:n.999-185T>C
ENST00000681746.1:c.1179-185T>C	ENSP00000505959.1:n.1179-185T>C
ENST00000320005.5:c.1179-185T>C	ENSP00000316605.5:n.1179-185T>C
NM_019098.4:c.1179-185T>C	NP_061971.3:n.1179-185T>C
XM_011517138.1:c.765-185T>C	XP_011515440.1:n.765-185T>C
XM_011517138.2:c.765-185T>C	XP_011515440.1:n.765-185T>C
NM_019098.5:c.1179-185T>C MANE Select	NP_061971.3:n.1179-185T>C