Canonical Allele Identifier: CA1116219173
Gene: CNGB3 HGNC NCBI

Linked Data

dbSNP Id: rs1823859892
gnomAD v3: 8-86671391-G-C
gnomAD v4: 8-86671391-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671391G>C , CM000670.2:g.86671391G>C GRCh38
NC_000008.10:g.87683619G>C , CM000670.1:g.87683619G>C GRCh37
NC_000008.9:g.87752735G>C NCBI36
NG_016980.1:g.77285C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.339-293C>G MANE Select ENSP00000316605.5:n.339-293C>G
ENST00000680314.1:n.100-293C>G
ENST00000681746.1:c.339-293C>G ENSP00000505959.1:n.339-293C>G
ENST00000320005.5:c.339-293C>G ENSP00000316605.5:n.339-293C>G
NM_019098.4:c.339-293C>G NP_061971.3:n.339-293C>G
XM_011517138.1:c.-76-293C>G XP_011515440.1:n.-76-293C>G
XM_011517138.2:c.-76-293C>G XP_011515440.1:n.-76-293C>G
NM_019098.5:c.339-293C>G MANE Select NP_061971.3:n.339-293C>G
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