Canonical Allele Identifier: CA1799890181
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739710A= , CM000670.2:g.86739710A= GRCh38
NC_000008.10:g.87751938A= , CM000670.1:g.87751938A= GRCh37
NC_000008.9:g.87821054A= NCBI36
NG_016980.1:g.8966T=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.156T= MANE Select ENSP00000316605.5:p.Ser52=
ENST00000681746.1:c.156T= ENSP00000505959.1:p.Ser52=
ENST00000320005.5:c.156T= ENSP00000316605.5:p.Ser52=
ENST00000519777.1:n.138T=
NM_019098.4:c.156T= NP_061971.3:p.Ser52=
NM_019098.5:c.156T= MANE Select NP_061971.3:p.Ser52=