Canonical Allele Identifier: CA371448300
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647880A>C , CM000670.2:g.86647880A>C GRCh38
NC_000008.10:g.87660108A>C , CM000670.1:g.87660108A>C GRCh37
NC_000008.9:g.87729224A>C NCBI36
NG_016980.1:g.100796T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.911T>G MANE Select ENSP00000316605.5:p.Val304Gly
ENST00000681546.1:n.731T>G
ENST00000681746.1:c.911T>G ENSP00000505959.1:p.Val304Gly
ENST00000320005.5:c.911T>G ENSP00000316605.5:p.Val304Gly
NM_019098.4:c.911T>G NP_061971.3:p.Val304Gly
XM_011517138.1:c.497T>G XP_011515440.1:p.Val166Gly
XM_011517138.2:c.497T>G XP_011515440.1:p.Val166Gly
NM_019098.5:c.911T>G MANE Select NP_061971.3:p.Val304Gly