Canonical Allele Identifier: CA1799829833
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647676A= , CM000670.2:g.86647676A= GRCh38
NC_000008.10:g.87659904A= , CM000670.1:g.87659904A= GRCh37
NC_000008.9:g.87729020A= NCBI36
NG_016980.1:g.101000T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.990+125T= MANE Select ENSP00000316605.5:n.990+125T=
ENST00000681546.1:n.810+125T=
ENST00000681746.1:c.990+125T= ENSP00000505959.1:n.990+125T=
ENST00000320005.5:c.990+125T= ENSP00000316605.5:n.990+125T=
NM_019098.4:c.990+125T= NP_061971.3:n.990+125T=
XM_011517138.1:c.576+125T= XP_011515440.1:n.576+125T=
XM_011517138.2:c.576+125T= XP_011515440.1:n.576+125T=
NM_019098.5:c.990+125T= MANE Select NP_061971.3:n.990+125T=