Canonical Allele Identifier: CA1799830491
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671494C= , CM000670.2:g.86671494C= GRCh38
NC_000008.10:g.87683722C= , CM000670.1:g.87683722C= GRCh37
NC_000008.9:g.87752838C= NCBI36
NG_016980.1:g.77182G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.339-396G= MANE Select ENSP00000316605.5:n.339-396G=
ENST00000680314.1:n.100-396G=
ENST00000681746.1:c.339-396G= ENSP00000505959.1:n.339-396G=
ENST00000320005.5:c.339-396G= ENSP00000316605.5:n.339-396G=
NM_019098.4:c.339-396G= NP_061971.3:n.339-396G=
XM_011517138.1:c.-76-396G= XP_011515440.1:n.-76-396G=
XM_011517138.2:c.-76-396G= XP_011515440.1:n.-76-396G=
NM_019098.5:c.339-396G= MANE Select NP_061971.3:n.339-396G=
Search 100 bp 5'
Search 100 bp 3'