Canonical Allele Identifier: CA371450108
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86670983C>G , CM000670.2:g.86670983C>G GRCh38
NC_000008.10:g.87683211C>G , CM000670.1:g.87683211C>G GRCh37
NC_000008.9:g.87752327C>G NCBI36
NG_016980.1:g.77693G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.454G>C MANE Select ENSP00000316605.5:p.Glu152Gln
ENST00000680314.1:n.215G>C
ENST00000681746.1:c.454G>C ENSP00000505959.1:p.Glu152Gln
ENST00000320005.5:c.454G>C ENSP00000316605.5:p.Glu152Gln
NM_019098.4:c.454G>C NP_061971.3:p.Glu152Gln
XM_011517138.1:c.40G>C XP_011515440.1:p.Glu14Gln
XM_011517138.2:c.40G>C XP_011515440.1:p.Glu14Gln
NM_019098.5:c.454G>C MANE Select NP_061971.3:p.Glu152Gln