Canonical Allele Identifier: CA1799829845
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1585990903
gnomAD v4: 8-86647681-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647681G>C , CM000670.2:g.86647681G>C GRCh38
NC_000008.10:g.87659909G>C , CM000670.1:g.87659909G>C GRCh37
NC_000008.9:g.87729025G>C NCBI36
NG_016980.1:g.100995C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.990+120C>G MANE Select ENSP00000316605.5:n.990+120C>G
ENST00000681546.1:n.810+120C>G
ENST00000681746.1:c.990+120C>G ENSP00000505959.1:n.990+120C>G
ENST00000320005.5:c.990+120C>G ENSP00000316605.5:n.990+120C>G
NM_019098.4:c.990+120C>G NP_061971.3:n.990+120C>G
XM_011517138.1:c.576+120C>G XP_011515440.1:n.576+120C>G
XM_011517138.2:c.576+120C>G XP_011515440.1:n.576+120C>G
NM_019098.5:c.990+120C>G MANE Select NP_061971.3:n.990+120C>G