Canonical Allele Identifier: CA371449868
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668100A>T , CM000670.2:g.86668100A>T GRCh38
NC_000008.10:g.87680328A>T , CM000670.1:g.87680328A>T GRCh37
NC_000008.9:g.87749444A>T NCBI36
NG_016980.1:g.80576T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.562T>A MANE Select ENSP00000316605.5:p.Leu188Met
ENST00000681746.1:c.562T>A ENSP00000505959.1:p.Leu188Met
ENST00000320005.5:c.562T>A ENSP00000316605.5:p.Leu188Met
NM_019098.4:c.562T>A NP_061971.3:p.Leu188Met
XM_011517138.1:c.148T>A XP_011515440.1:p.Leu50Met
XM_011517138.2:c.148T>A XP_011515440.1:p.Leu50Met
NM_019098.5:c.562T>A MANE Select NP_061971.3:p.Leu188Met