Canonical Allele Identifier: CA1799829907
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671040G= , CM000670.2:g.86671040G= GRCh38
NC_000008.10:g.87683268G= , CM000670.1:g.87683268G= GRCh37
NC_000008.9:g.87752384G= NCBI36
NG_016980.1:g.77636C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.397C= MANE Select ENSP00000316605.5:p.His133=
ENST00000680314.1:n.158C=
ENST00000681746.1:c.397C= ENSP00000505959.1:p.His133=
ENST00000320005.5:c.397C= ENSP00000316605.5:p.His133=
NM_019098.4:c.397C= NP_061971.3:p.His133=
XM_011517138.1:c.-18C= XP_011515440.1:n.-18C=
XM_011517138.2:c.-18C= XP_011515440.1:n.-18C=
NM_019098.5:c.397C= MANE Select NP_061971.3:p.His133=