Canonical Allele Identifier: CA1799829989
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671067T= , CM000670.2:g.86671067T= GRCh38
NC_000008.10:g.87683295T= , CM000670.1:g.87683295T= GRCh37
NC_000008.9:g.87752411T= NCBI36
NG_016980.1:g.77609A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.370A= MANE Select ENSP00000316605.5:p.Ile124=
ENST00000680314.1:n.131A=
ENST00000681746.1:c.370A= ENSP00000505959.1:p.Ile124=
ENST00000320005.5:c.370A= ENSP00000316605.5:p.Ile124=
NM_019098.4:c.370A= NP_061971.3:p.Ile124=
XM_011517138.1:c.-45A= XP_011515440.1:n.-45A=
XM_011517138.2:c.-45A= XP_011515440.1:n.-45A=
NM_019098.5:c.370A= MANE Select NP_061971.3:p.Ile124=