Canonical Allele Identifier: CA1799830449

Gene: CNGB3

Linked Data

• dbSNP Id: rs1823860815

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86671448T>C , CM000670.2:g.86671448T>C	GRCh38
NC_000008.10:g.87683676T>C , CM000670.1:g.87683676T>C	GRCh37
NC_000008.9:g.87752792T>C	NCBI36
NG_016980.1:g.77228A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.339-350A>G MANE Select	ENSP00000316605.5:n.339-350A>G
ENST00000680314.1:n.100-350A>G
ENST00000681746.1:c.339-350A>G	ENSP00000505959.1:n.339-350A>G
ENST00000320005.5:c.339-350A>G	ENSP00000316605.5:n.339-350A>G
NM_019098.4:c.339-350A>G	NP_061971.3:n.339-350A>G
XM_011517138.1:c.-76-350A>G	XP_011515440.1:n.-76-350A>G
XM_011517138.2:c.-76-350A>G	XP_011515440.1:n.-76-350A>G
NM_019098.5:c.339-350A>G MANE Select	NP_061971.3:n.339-350A>G