Canonical Allele Identifier: CA2579200069
Gene: CNGB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647777G>A , CM000670.2:g.86647777G>A GRCh38
NC_000008.10:g.87660005G>A , CM000670.1:g.87660005G>A GRCh37
NC_000008.9:g.87729121G>A NCBI36
NG_016980.1:g.100899C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.990+24C>T MANE Select ENSP00000316605.5:n.990+24C>T
ENST00000681546.1:n.810+24C>T
ENST00000681746.1:c.990+24C>T ENSP00000505959.1:n.990+24C>T
ENST00000320005.5:c.990+24C>T ENSP00000316605.5:n.990+24C>T
NM_019098.4:c.990+24C>T NP_061971.3:n.990+24C>T
XM_011517138.1:c.576+24C>T XP_011515440.1:n.576+24C>T
XM_011517138.2:c.576+24C>T XP_011515440.1:n.576+24C>T
NM_019098.5:c.990+24C>T MANE Select NP_061971.3:n.990+24C>T