Canonical Allele Identifier: CA1799789631
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579211A= , CM000670.2:g.86579211A= GRCh38
NC_000008.10:g.87591439A= , CM000670.1:g.87591439A= GRCh37
NC_000008.9:g.87660555A= NCBI36
NG_016980.1:g.169465T=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1823T= MANE Select ENSP00000316605.5:p.Val608=
ENST00000681546.1:n.1643T=
ENST00000681746.1:c.*234T= ENSP00000505959.1:n.*234T=
ENST00000320005.5:c.1823T= ENSP00000316605.5:p.Val608=
NM_019098.4:c.1823T= NP_061971.3:p.Val608=
XM_011517138.1:c.1409T= XP_011515440.1:p.Val470=
XM_011517138.2:c.1409T= XP_011515440.1:p.Val470=
NM_019098.5:c.1823T= MANE Select NP_061971.3:p.Val608=