Canonical Allele Identifier: CA2717721408
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs2131597243

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647713T>C , CM000670.2:g.86647713T>C GRCh38
NC_000008.10:g.87659941T>C , CM000670.1:g.87659941T>C GRCh37
NC_000008.9:g.87729057T>C NCBI36
NG_016980.1:g.100963A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.990+88A>G MANE Select ENSP00000316605.5:n.990+88A>G
ENST00000681546.1:n.810+88A>G
ENST00000681746.1:c.990+88A>G ENSP00000505959.1:n.990+88A>G
ENST00000320005.5:c.990+88A>G ENSP00000316605.5:n.990+88A>G
NM_019098.4:c.990+88A>G NP_061971.3:n.990+88A>G
XM_011517138.1:c.576+88A>G XP_011515440.1:n.576+88A>G
XM_011517138.2:c.576+88A>G XP_011515440.1:n.576+88A>G
NM_019098.5:c.990+88A>G MANE Select NP_061971.3:n.990+88A>G