Canonical Allele Identifier: CA461816100
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87660032T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647804T>C , CM000670.2:g.86647804T>C GRCh38
NC_000008.10:g.87660032T>C , CM000670.1:g.87660032T>C GRCh37
NC_000008.9:g.87729148T>C NCBI36
NG_016980.1:g.100872A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.987A>G MANE Select ENSP00000316605.5:p.Leu329=
ENST00000681546.1:n.807A>G
ENST00000681746.1:c.987A>G ENSP00000505959.1:p.Leu329=
ENST00000320005.5:c.987A>G ENSP00000316605.5:p.Leu329=
NM_019098.4:c.987A>G NP_061971.3:p.Leu329=
XM_011517138.1:c.573A>G XP_011515440.1:p.Leu191=
XM_011517138.2:c.573A>G XP_011515440.1:p.Leu191=
NM_019098.5:c.987A>G MANE Select NP_061971.3:p.Leu329=