Canonical Allele Identifier: CA1799788756
Gene: CNGB3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86578866G= , CM000670.2:g.86578866G= GRCh38
NC_000008.10:g.87591094G= , CM000670.1:g.87591094G= GRCh37
NC_000008.9:g.87660210G= NCBI36
NG_016980.1:g.169810C=

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1929-3C= MANE Select ENSP00000316605.5:n.1929-3C=
ENST00000681546.1:n.1749-3C=
ENST00000681746.1:c.*340-3C= ENSP00000505959.1:n.*340-3C=
ENST00000320005.5:c.1929-3C= ENSP00000316605.5:n.1929-3C=
ENST00000517327.5:c.102-3C= ENSP00000428329.1:n.102-3C=
NM_019098.4:c.1929-3C= NP_061971.3:n.1929-3C=
XM_011517138.1:c.1515-3C= XP_011515440.1:n.1515-3C=
XM_011517138.2:c.1515-3C= XP_011515440.1:n.1515-3C=
NM_019098.5:c.1929-3C= MANE Select NP_061971.3:n.1929-3C=
Search 100 bp 5'
Search 100 bp 3'