Canonical Allele Identifier: CA2781156164
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86667159_86667160insACG , CM000670.2:g.86667159_86667160insACG GRCh38
NC_000008.10:g.87679387_87679388insACG , CM000670.1:g.87679387_87679388insACG GRCh37
NC_000008.9:g.87748503_87748504insACG NCBI36
NG_016980.1:g.81516_81517insCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.644-27_644-26insCGT MANE Select ENSP00000316605.5:n.644-27_644-26insCGT
ENST00000681746.1:c.644-27_644-26insCGT ENSP00000505959.1:n.644-27_644-26insCGT
ENST00000320005.5:c.644-27_644-26insCGT ENSP00000316605.5:n.644-27_644-26insCGT
NM_019098.4:c.644-27_644-26insCGT NP_061971.3:n.644-27_644-26insCGT
XM_011517138.1:c.230-27_230-26insCGT XP_011515440.1:n.230-27_230-26insCGT
XM_011517138.2:c.230-27_230-26insCGT XP_011515440.1:n.230-27_230-26insCGT
NM_019098.5:c.644-27_644-26insCGT MANE Select NP_061971.3:n.644-27_644-26insCGT
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