Canonical Allele Identifier: CA2579200059
Gene: CNGB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647714A>G , CM000670.2:g.86647714A>G GRCh38
NC_000008.10:g.87659942A>G , CM000670.1:g.87659942A>G GRCh37
NC_000008.9:g.87729058A>G NCBI36
NG_016980.1:g.100962T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.990+87T>C MANE Select ENSP00000316605.5:n.990+87T>C
ENST00000681546.1:n.810+87T>C
ENST00000681746.1:c.990+87T>C ENSP00000505959.1:n.990+87T>C
ENST00000320005.5:c.990+87T>C ENSP00000316605.5:n.990+87T>C
NM_019098.4:c.990+87T>C NP_061971.3:n.990+87T>C
XM_011517138.1:c.576+87T>C XP_011515440.1:n.576+87T>C
XM_011517138.2:c.576+87T>C XP_011515440.1:n.576+87T>C
NM_019098.5:c.990+87T>C MANE Select NP_061971.3:n.990+87T>C
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