Canonical Allele Identifier: CA4800318
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs760143650
gnomAD v2: 8-87679377-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86667149G>A , CM000670.2:g.86667149G>A GRCh38
NC_000008.10:g.87679377G>A , CM000670.1:g.87679377G>A GRCh37
NC_000008.9:g.87748493G>A NCBI36
NG_016980.1:g.81527C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.644-16C>T MANE Select ENSP00000316605.5:n.644-16C>T
ENST00000681746.1:c.644-16C>T ENSP00000505959.1:n.644-16C>T
ENST00000320005.5:c.644-16C>T ENSP00000316605.5:n.644-16C>T
NM_019098.4:c.644-16C>T NP_061971.3:n.644-16C>T
XM_011517138.1:c.230-16C>T XP_011515440.1:n.230-16C>T
XM_011517138.2:c.230-16C>T XP_011515440.1:n.230-16C>T
NM_019098.5:c.644-16C>T MANE Select NP_061971.3:n.644-16C>T