Canonical Allele Identifier: CA1799829726
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86670987C= , CM000670.2:g.86670987C= GRCh38
NC_000008.10:g.87683215C= , CM000670.1:g.87683215C= GRCh37
NC_000008.9:g.87752331C= NCBI36
NG_016980.1:g.77689G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.450G= MANE Select ENSP00000316605.5:p.Leu150=
ENST00000680314.1:n.211G=
ENST00000681746.1:c.450G= ENSP00000505959.1:p.Leu150=
ENST00000320005.5:c.450G= ENSP00000316605.5:p.Leu150=
NM_019098.4:c.450G= NP_061971.3:p.Leu150=
XM_011517138.1:c.36G= XP_011515440.1:p.Leu12=
XM_011517138.2:c.36G= XP_011515440.1:p.Leu12=
NM_019098.5:c.450G= MANE Select NP_061971.3:p.Leu150=