Canonical Allele Identifier: CA1799781585
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1821612350

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86574100G>A , CM000670.2:g.86574100G>A GRCh38
NC_000008.10:g.87586328G>A , CM000670.1:g.87586328G>A GRCh37
NC_000008.9:g.87655444G>A NCBI36
NG_016980.1:g.174576C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000681746.1:c.*2545C>T ENSP00000505959.1:n.*2545C>T
ENST00000320005.5:c.*1704C>T ENSP00000316605.5:n.*1704C>T
ENST00000517327.5:c.276+4589C>T ENSP00000428329.1:n.276+4589C>T
NM_019098.4:c.*1704C>T NP_061971.3:n.*1704C>T
XM_011517138.1:c.*1704C>T XP_011515440.1:n.*1704C>T
XM_011517138.2:c.*1704C>T XP_011515440.1:n.*1704C>T