Canonical Allele Identifier: CA461978635
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87751947T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739719T>C , CM000670.2:g.86739719T>C GRCh38
NC_000008.10:g.87751947T>C , CM000670.1:g.87751947T>C GRCh37
NC_000008.9:g.87821063T>C NCBI36
NG_016980.1:g.8957A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.147A>G MANE Select ENSP00000316605.5:p.Glu49=
ENST00000681746.1:c.147A>G ENSP00000505959.1:p.Glu49=
ENST00000320005.5:c.147A>G ENSP00000316605.5:p.Glu49=
ENST00000519777.1:n.129A>G
NM_019098.4:c.147A>G NP_061971.3:p.Glu49=
NM_019098.5:c.147A>G MANE Select NP_061971.3:p.Glu49=