Canonical Allele Identifier: CA371449873
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668103G>T , CM000670.2:g.86668103G>T GRCh38
NC_000008.10:g.87680331G>T , CM000670.1:g.87680331G>T GRCh37
NC_000008.9:g.87749447G>T NCBI36
NG_016980.1:g.80573C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.559C>A MANE Select ENSP00000316605.5:p.Leu187Met
ENST00000681746.1:c.559C>A ENSP00000505959.1:p.Leu187Met
ENST00000320005.5:c.559C>A ENSP00000316605.5:p.Leu187Met
NM_019098.4:c.559C>A NP_061971.3:p.Leu187Met
XM_011517138.1:c.145C>A XP_011515440.1:p.Leu49Met
XM_011517138.2:c.145C>A XP_011515440.1:p.Leu49Met
NM_019098.5:c.559C>A MANE Select NP_061971.3:p.Leu187Met