Canonical Allele Identifier: CA1799785083
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86576299C= , CM000670.2:g.86576299C= GRCh38
NC_000008.10:g.87588527C= , CM000670.1:g.87588527C= GRCh37
NC_000008.9:g.87657643C= NCBI36
NG_016980.1:g.172377G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320005.6:c.2104-169G= MANE Select ENSP00000316605.5:n.2104-169G=
ENST00000681546.1:n.1924-169G=
ENST00000681746.1:c.*515-169G= ENSP00000505959.1:n.*515-169G=
ENST00000320005.5:c.2104-169G= ENSP00000316605.5:n.2104-169G=
ENST00000517327.5:c.276+2390G= ENSP00000428329.1:n.276+2390G=
NM_019098.4:c.2104-169G= NP_061971.3:n.2104-169G=
XM_011517138.1:c.1690-169G= XP_011515440.1:n.1690-169G=
XM_011517138.2:c.1690-169G= XP_011515440.1:n.1690-169G=
NM_019098.5:c.2104-169G= MANE Select NP_061971.3:n.2104-169G=
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