Canonical Allele Identifier: CA1799825602
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86643728T= , CM000670.2:g.86643728T= GRCh38
NC_000008.10:g.87655956T= , CM000670.1:g.87655956T= GRCh37
NC_000008.9:g.87725072T= NCBI36
NG_016980.1:g.104948A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.1178+23A= MANE Select ENSP00000316605.5:n.1178+23A=
ENST00000681546.1:n.998+23A=
ENST00000681746.1:c.1178+23A= ENSP00000505959.1:n.1178+23A=
ENST00000320005.5:c.1178+23A= ENSP00000316605.5:n.1178+23A=
NM_019098.4:c.1178+23A= NP_061971.3:n.1178+23A=
XM_011517138.1:c.764+23A= XP_011515440.1:n.764+23A=
XM_011517138.2:c.764+23A= XP_011515440.1:n.764+23A=
NM_019098.5:c.1178+23A= MANE Select NP_061971.3:n.1178+23A=
Search 100 bp 5'
Search 100 bp 3'