Canonical Allele Identifier: CA2687823586
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86575774-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575774G>T , CM000670.2:g.86575774G>T GRCh38
NC_000008.10:g.87588002G>T , CM000670.1:g.87588002G>T GRCh37
NC_000008.9:g.87657118G>T NCBI36
NG_016980.1:g.172902C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.*30C>A MANE Select ENSP00000316605.5:n.*30C>A
ENST00000681546.1:n.2280C>A
ENST00000681746.1:c.*871C>A ENSP00000505959.1:n.*871C>A
ENST00000320005.5:c.*30C>A ENSP00000316605.5:n.*30C>A
ENST00000517327.5:c.276+2915C>A ENSP00000428329.1:n.276+2915C>A
NM_019098.4:c.*30C>A NP_061971.3:n.*30C>A
XM_011517138.1:c.*30C>A XP_011515440.1:n.*30C>A
XM_011517138.2:c.*30C>A XP_011515440.1:n.*30C>A
NM_019098.5:c.*30C>A MANE Select NP_061971.3:n.*30C>A
Search 100 bp 5'
Search 100 bp 3'