Canonical Allele Identifier: CA1799826121
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86667947G= , CM000670.2:g.86667947G= GRCh38
NC_000008.10:g.87680175G= , CM000670.1:g.87680175G= GRCh37
NC_000008.9:g.87749291G= NCBI36
NG_016980.1:g.80729C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.643+72C= MANE Select ENSP00000316605.5:n.643+72C=
ENST00000681746.1:c.643+72C= ENSP00000505959.1:n.643+72C=
ENST00000320005.5:c.643+72C= ENSP00000316605.5:n.643+72C=
NM_019098.4:c.643+72C= NP_061971.3:n.643+72C=
XM_011517138.1:c.229+72C= XP_011515440.1:n.229+72C=
XM_011517138.2:c.229+72C= XP_011515440.1:n.229+72C=
NM_019098.5:c.643+72C= MANE Select NP_061971.3:n.643+72C=
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