Canonical Allele Identifier: CA1799826482
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668197C= , CM000670.2:g.86668197C= GRCh38
NC_000008.10:g.87680425C= , CM000670.1:g.87680425C= GRCh37
NC_000008.9:g.87749541C= NCBI36
NG_016980.1:g.80479G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.494-29G= MANE Select ENSP00000316605.5:n.494-29G=
ENST00000680314.1:n.255-29G=
ENST00000681746.1:c.494-29G= ENSP00000505959.1:n.494-29G=
ENST00000320005.5:c.494-29G= ENSP00000316605.5:n.494-29G=
NM_019098.4:c.494-29G= NP_061971.3:n.494-29G=
XM_011517138.1:c.80-29G= XP_011515440.1:n.80-29G=
XM_011517138.2:c.80-29G= XP_011515440.1:n.80-29G=
NM_019098.5:c.494-29G= MANE Select NP_061971.3:n.494-29G=
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