Canonical Allele Identifier: CA1799826297
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668106T= , CM000670.2:g.86668106T= GRCh38
NC_000008.10:g.87680334T= , CM000670.1:g.87680334T= GRCh37
NC_000008.9:g.87749450T= NCBI36
NG_016980.1:g.80570A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.556A= MANE Select ENSP00000316605.5:p.Arg186=
ENST00000681746.1:c.556A= ENSP00000505959.1:p.Arg186=
ENST00000320005.5:c.556A= ENSP00000316605.5:p.Arg186=
NM_019098.4:c.556A= NP_061971.3:p.Arg186=
XM_011517138.1:c.142A= XP_011515440.1:p.Arg48=
XM_011517138.2:c.142A= XP_011515440.1:p.Arg48=
NM_019098.5:c.556A= MANE Select NP_061971.3:p.Arg186=