Canonical Allele Identifier: CA371444089
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86632781C>T , CM000670.2:g.86632781C>T GRCh38
NC_000008.10:g.87645009C>T , CM000670.1:g.87645009C>T GRCh37
NC_000008.9:g.87714125C>T NCBI36
NG_016980.1:g.115895G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1291G>A MANE Select ENSP00000316605.5:p.Val431Ile
ENST00000681546.1:n.1111G>A
ENST00000681746.1:c.1291G>A ENSP00000505959.1:p.Val431Ile
ENST00000320005.5:c.1291G>A ENSP00000316605.5:p.Val431Ile
NM_019098.4:c.1291G>A NP_061971.3:p.Val431Ile
XM_011517138.1:c.877G>A XP_011515440.1:p.Val293Ile
XM_011517138.2:c.877G>A XP_011515440.1:p.Val293Ile
NM_019098.5:c.1291G>A MANE Select NP_061971.3:p.Val431Ile