Canonical Allele Identifier: CA461978630
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87751935G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739707G>A , CM000670.2:g.86739707G>A GRCh38
NC_000008.10:g.87751935G>A , CM000670.1:g.87751935G>A GRCh37
NC_000008.9:g.87821051G>A NCBI36
NG_016980.1:g.8969C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.159C>T MANE Select ENSP00000316605.5:p.Leu53=
ENST00000681746.1:c.159C>T ENSP00000505959.1:p.Leu53=
ENST00000320005.5:c.159C>T ENSP00000316605.5:p.Leu53=
ENST00000519777.1:n.141C>T
NM_019098.4:c.159C>T NP_061971.3:p.Leu53=
NM_019098.5:c.159C>T MANE Select NP_061971.3:p.Leu53=