Canonical Allele Identifier: CA1799830427
Gene: CNGB3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671432C= , CM000670.2:g.86671432C= GRCh38
NC_000008.10:g.87683660C= , CM000670.1:g.87683660C= GRCh37
NC_000008.9:g.87752776C= NCBI36
NG_016980.1:g.77244G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.339-334G= MANE Select ENSP00000316605.5:n.339-334G=
ENST00000680314.1:n.100-334G=
ENST00000681746.1:c.339-334G= ENSP00000505959.1:n.339-334G=
ENST00000320005.5:c.339-334G= ENSP00000316605.5:n.339-334G=
NM_019098.4:c.339-334G= NP_061971.3:n.339-334G=
XM_011517138.1:c.-76-334G= XP_011515440.1:n.-76-334G=
XM_011517138.2:c.-76-334G= XP_011515440.1:n.-76-334G=
NM_019098.5:c.339-334G= MANE Select NP_061971.3:n.339-334G=
Search 100 bp 5'
Search 100 bp 3'