Canonical Allele Identifier: CA371446303
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575973G>A , CM000670.2:g.86575973G>A GRCh38
NC_000008.10:g.87588201G>A , CM000670.1:g.87588201G>A GRCh37
NC_000008.9:g.87657317G>A NCBI36
NG_016980.1:g.172703C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2261C>T MANE Select ENSP00000316605.5:p.Pro754Leu
ENST00000681546.1:n.2081C>T
ENST00000681746.1:c.*672C>T ENSP00000505959.1:n.*672C>T
ENST00000320005.5:c.2261C>T ENSP00000316605.5:p.Pro754Leu
ENST00000517327.5:c.276+2716C>T ENSP00000428329.1:n.276+2716C>T
NM_019098.4:c.2261C>T NP_061971.3:p.Pro754Leu
XM_011517138.1:c.1847C>T XP_011515440.1:p.Pro616Leu
XM_011517138.2:c.1847C>T XP_011515440.1:p.Pro616Leu
NM_019098.5:c.2261C>T MANE Select NP_061971.3:p.Pro754Leu