Canonical Allele Identifier: CA1799890257
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86739774T= , CM000670.2:g.86739774T= GRCh38
NC_000008.10:g.87752002T= , CM000670.1:g.87752002T= GRCh37
NC_000008.9:g.87821118T= NCBI36
NG_016980.1:g.8902A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.130-38A= MANE Select ENSP00000316605.5:n.130-38A=
ENST00000681746.1:c.130-38A= ENSP00000505959.1:n.130-38A=
ENST00000320005.5:c.130-38A= ENSP00000316605.5:n.130-38A=
ENST00000519777.1:n.112-38A=
NM_019098.4:c.130-38A= NP_061971.3:n.130-38A=
NM_019098.5:c.130-38A= MANE Select NP_061971.3:n.130-38A=