Canonical Allele Identifier: CA1799830474
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86671473T= , CM000670.2:g.86671473T= GRCh38
NC_000008.10:g.87683701T= , CM000670.1:g.87683701T= GRCh37
NC_000008.9:g.87752817T= NCBI36
NG_016980.1:g.77203A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.339-375A= MANE Select ENSP00000316605.5:n.339-375A=
ENST00000680314.1:n.100-375A=
ENST00000681746.1:c.339-375A= ENSP00000505959.1:n.339-375A=
ENST00000320005.5:c.339-375A= ENSP00000316605.5:n.339-375A=
NM_019098.4:c.339-375A= NP_061971.3:n.339-375A=
XM_011517138.1:c.-76-375A= XP_011515440.1:n.-76-375A=
XM_011517138.2:c.-76-375A= XP_011515440.1:n.-76-375A=
NM_019098.5:c.339-375A= MANE Select NP_061971.3:n.339-375A=
Search 100 bp 5'
Search 100 bp 3'