Canonical Allele Identifier: CA1799825465
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86643480T= , CM000670.2:g.86643480T= GRCh38
NC_000008.10:g.87655708T= , CM000670.1:g.87655708T= GRCh37
NC_000008.9:g.87724824T= NCBI36
NG_016980.1:g.105196A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.1178+271A= MANE Select ENSP00000316605.5:n.1178+271A=
ENST00000681546.1:n.998+271A=
ENST00000681746.1:c.1178+271A= ENSP00000505959.1:n.1178+271A=
ENST00000320005.5:c.1178+271A= ENSP00000316605.5:n.1178+271A=
NM_019098.4:c.1178+271A= NP_061971.3:n.1178+271A=
XM_011517138.1:c.764+271A= XP_011515440.1:n.764+271A=
XM_011517138.2:c.764+271A= XP_011515440.1:n.764+271A=
NM_019098.5:c.1178+271A= MANE Select NP_061971.3:n.1178+271A=
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