Canonical Allele Identifier: CA1799830212
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647879G= , CM000670.2:g.86647879G= GRCh38
NC_000008.10:g.87660107G= , CM000670.1:g.87660107G= GRCh37
NC_000008.9:g.87729223G= NCBI36
NG_016980.1:g.100797C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.912C= MANE Select ENSP00000316605.5:p.Val304=
ENST00000681546.1:n.732C=
ENST00000681746.1:c.912C= ENSP00000505959.1:p.Val304=
ENST00000320005.5:c.912C= ENSP00000316605.5:p.Val304=
NM_019098.4:c.912C= NP_061971.3:p.Val304=
XM_011517138.1:c.498C= XP_011515440.1:p.Val166=
XM_011517138.2:c.498C= XP_011515440.1:p.Val166=
NM_019098.5:c.912C= MANE Select NP_061971.3:p.Val304=