Canonical Allele Identifier: CA1799825601
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86667136G= , CM000670.2:g.86667136G= GRCh38
NC_000008.10:g.87679364G= , CM000670.1:g.87679364G= GRCh37
NC_000008.9:g.87748480G= NCBI36
NG_016980.1:g.81540C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.644-3C= MANE Select ENSP00000316605.5:n.644-3C=
ENST00000681746.1:c.644-3C= ENSP00000505959.1:n.644-3C=
ENST00000320005.5:c.644-3C= ENSP00000316605.5:n.644-3C=
NM_019098.4:c.644-3C= NP_061971.3:n.644-3C=
XM_011517138.1:c.230-3C= XP_011515440.1:n.230-3C=
XM_011517138.2:c.230-3C= XP_011515440.1:n.230-3C=
NM_019098.5:c.644-3C= MANE Select NP_061971.3:n.644-3C=