Canonical Allele Identifier: CA1799830168
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647873T= , CM000670.2:g.86647873T= GRCh38
NC_000008.10:g.87660101T= , CM000670.1:g.87660101T= GRCh37
NC_000008.9:g.87729217T= NCBI36
NG_016980.1:g.100803A=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.918A= MANE Select ENSP00000316605.5:p.Ser306=
ENST00000681546.1:n.738A=
ENST00000681746.1:c.918A= ENSP00000505959.1:p.Ser306=
ENST00000320005.5:c.918A= ENSP00000316605.5:p.Ser306=
NM_019098.4:c.918A= NP_061971.3:p.Ser306=
XM_011517138.1:c.504A= XP_011515440.1:p.Ser168=
XM_011517138.2:c.504A= XP_011515440.1:p.Ser168=
NM_019098.5:c.918A= MANE Select NP_061971.3:p.Ser306=