Canonical Allele Identifier: CA1799825624
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86667163A= , CM000670.2:g.86667163A= GRCh38
NC_000008.10:g.87679391A= , CM000670.1:g.87679391A= GRCh37
NC_000008.9:g.87748507A= NCBI36
NG_016980.1:g.81513T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.644-30T= MANE Select ENSP00000316605.5:n.644-30T=
ENST00000681746.1:c.644-30T= ENSP00000505959.1:n.644-30T=
ENST00000320005.5:c.644-30T= ENSP00000316605.5:n.644-30T=
NM_019098.4:c.644-30T= NP_061971.3:n.644-30T=
XM_011517138.1:c.230-30T= XP_011515440.1:n.230-30T=
XM_011517138.2:c.230-30T= XP_011515440.1:n.230-30T=
NM_019098.5:c.644-30T= MANE Select NP_061971.3:n.644-30T=
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