Canonical Allele Identifier: CA582921381
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1410849607
gnomAD v2: 8-87683586-T-C
MyVariant Identifiers: chr8:g.87683586T>C (hg19) chr8:g.86671358T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671358T>C , CM000670.2:g.86671358T>C GRCh38
NC_000008.10:g.87683586T>C , CM000670.1:g.87683586T>C GRCh37
NC_000008.9:g.87752702T>C NCBI36
NG_016980.1:g.77318A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.339-260A>G MANE Select ENSP00000316605.5:n.339-260A>G
ENST00000680314.1:n.100-260A>G
ENST00000681746.1:c.339-260A>G ENSP00000505959.1:n.339-260A>G
ENST00000320005.5:c.339-260A>G ENSP00000316605.5:n.339-260A>G
NM_019098.4:c.339-260A>G NP_061971.3:n.339-260A>G
XM_011517138.1:c.-76-260A>G XP_011515440.1:n.-76-260A>G
XM_011517138.2:c.-76-260A>G XP_011515440.1:n.-76-260A>G
NM_019098.5:c.339-260A>G MANE Select NP_061971.3:n.339-260A>G
Search 100 bp 5'
Search 100 bp 3'