Canonical Allele Identifier: CA1799890183
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739711G= , CM000670.2:g.86739711G= GRCh38
NC_000008.10:g.87751939G= , CM000670.1:g.87751939G= GRCh37
NC_000008.9:g.87821055G= NCBI36
NG_016980.1:g.8965C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.155C= MANE Select ENSP00000316605.5:p.Ser52=
ENST00000681746.1:c.155C= ENSP00000505959.1:p.Ser52=
ENST00000320005.5:c.155C= ENSP00000316605.5:p.Ser52=
ENST00000519777.1:n.137C=
NM_019098.4:c.155C= NP_061971.3:p.Ser52=
NM_019098.5:c.155C= MANE Select NP_061971.3:p.Ser52=
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