Canonical Allele Identifier: CA371449681
Gene: CNGB3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.87679362C>T (hg19) chr8:g.86667134C>T (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.644-1G>A MANE Select ENSP00000316605.5:n.644-1G>A
ENST00000681746.1:c.644-1G>A ENSP00000505959.1:n.644-1G>A
ENST00000320005.5:c.644-1G>A ENSP00000316605.5:n.644-1G>A
NM_019098.4:c.644-1G>A NP_061971.3:n.644-1G>A
XM_011517138.1:c.230-1G>A XP_011515440.1:n.230-1G>A
XM_011517138.2:c.230-1G>A XP_011515440.1:n.230-1G>A
NM_019098.5:c.644-1G>A MANE Select NP_061971.3:n.644-1G>A
Search 100 bp 5'
Search 100 bp 3'