Canonical Allele Identifier: CA371449877
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668105C>G , CM000670.2:g.86668105C>G GRCh38
NC_000008.10:g.87680333C>G , CM000670.1:g.87680333C>G GRCh37
NC_000008.9:g.87749449C>G NCBI36
NG_016980.1:g.80571G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.557G>C MANE Select ENSP00000316605.5:p.Arg186Thr
ENST00000681746.1:c.557G>C ENSP00000505959.1:p.Arg186Thr
ENST00000320005.5:c.557G>C ENSP00000316605.5:p.Arg186Thr
NM_019098.4:c.557G>C NP_061971.3:p.Arg186Thr
XM_011517138.1:c.143G>C XP_011515440.1:p.Arg48Thr
XM_011517138.2:c.143G>C XP_011515440.1:p.Arg48Thr
NM_019098.5:c.557G>C MANE Select NP_061971.3:p.Arg186Thr