Canonical Allele Identifier: CA371449680
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86667134-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86667134C>A , CM000670.2:g.86667134C>A GRCh38
NC_000008.10:g.87679362C>A , CM000670.1:g.87679362C>A GRCh37
NC_000008.9:g.87748478C>A NCBI36
NG_016980.1:g.81542G>T

Transcript Alleles

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