Canonical Allele Identifier: CA1799782231
Gene: CNGB3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86574503A= , CM000670.2:g.86574503A= GRCh38
NC_000008.10:g.87586731A= , CM000670.1:g.87586731A= GRCh37
NC_000008.9:g.87655847A= NCBI36
NG_016980.1:g.174173T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.*1301T= MANE Select ENSP00000316605.5:n.*1301T=
ENST00000681546.1:n.3551T=
ENST00000681746.1:c.*2142T= ENSP00000505959.1:n.*2142T=
ENST00000320005.5:c.*1301T= ENSP00000316605.5:n.*1301T=
ENST00000517327.5:c.276+4186T= ENSP00000428329.1:n.276+4186T=
NM_019098.4:c.*1301T= NP_061971.3:n.*1301T=
XM_011517138.1:c.*1301T= XP_011515440.1:n.*1301T=
XM_011517138.2:c.*1301T= XP_011515440.1:n.*1301T=
NM_019098.5:c.*1301T= MANE Select NP_061971.3:n.*1301T=
Search 100 bp 5'
Search 100 bp 3'