Canonical Allele Identifier: CA371450236
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671043G>T , CM000670.2:g.86671043G>T GRCh38
NC_000008.10:g.87683271G>T , CM000670.1:g.87683271G>T GRCh37
NC_000008.9:g.87752387G>T NCBI36
NG_016980.1:g.77633C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.394C>A MANE Select ENSP00000316605.5:p.Leu132Ile
ENST00000680314.1:n.155C>A
ENST00000681746.1:c.394C>A ENSP00000505959.1:p.Leu132Ile
ENST00000320005.5:c.394C>A ENSP00000316605.5:p.Leu132Ile
NM_019098.4:c.394C>A NP_061971.3:p.Leu132Ile
XM_011517138.1:c.-21C>A XP_011515440.1:n.-21C>A
XM_011517138.2:c.-21C>A XP_011515440.1:n.-21C>A
NM_019098.5:c.394C>A MANE Select NP_061971.3:p.Leu132Ile