Canonical Allele Identifier: CA371446310
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575975T>G , CM000670.2:g.86575975T>G GRCh38
NC_000008.10:g.87588203T>G , CM000670.1:g.87588203T>G GRCh37
NC_000008.9:g.87657319T>G NCBI36
NG_016980.1:g.172701A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2259A>C MANE Select ENSP00000316605.5:p.Arg753Ser
ENST00000681546.1:n.2079A>C
ENST00000681746.1:c.*670A>C ENSP00000505959.1:n.*670A>C
ENST00000320005.5:c.2259A>C ENSP00000316605.5:p.Arg753Ser
ENST00000517327.5:c.276+2714A>C ENSP00000428329.1:n.276+2714A>C
NM_019098.4:c.2259A>C NP_061971.3:p.Arg753Ser
XM_011517138.1:c.1845A>C XP_011515440.1:p.Arg615Ser
XM_011517138.2:c.1845A>C XP_011515440.1:p.Arg615Ser
NM_019098.5:c.2259A>C MANE Select NP_061971.3:p.Arg753Ser