Canonical Allele Identifier: CA1799868889
Gene: CNGB3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86633062T= , CM000670.2:g.86633062T= GRCh38
NC_000008.10:g.87645290T= , CM000670.1:g.87645290T= GRCh37
NC_000008.9:g.87714406T= NCBI36
NG_016980.1:g.115614A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.1179-169A= MANE Select ENSP00000316605.5:n.1179-169A=
ENST00000681546.1:n.999-169A=
ENST00000681746.1:c.1179-169A= ENSP00000505959.1:n.1179-169A=
ENST00000320005.5:c.1179-169A= ENSP00000316605.5:n.1179-169A=
NM_019098.4:c.1179-169A= NP_061971.3:n.1179-169A=
XM_011517138.1:c.765-169A= XP_011515440.1:n.765-169A=
XM_011517138.2:c.765-169A= XP_011515440.1:n.765-169A=
NM_019098.5:c.1179-169A= MANE Select NP_061971.3:n.1179-169A=
Search 100 bp 5'
Search 100 bp 3'