Canonical Allele Identifier: CA371449901
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668114T>G , CM000670.2:g.86668114T>G GRCh38
NC_000008.10:g.87680342T>G , CM000670.1:g.87680342T>G GRCh37
NC_000008.9:g.87749458T>G NCBI36
NG_016980.1:g.80562A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.548A>C MANE Select ENSP00000316605.5:p.His183Pro
ENST00000681746.1:c.548A>C ENSP00000505959.1:p.His183Pro
ENST00000320005.5:c.548A>C ENSP00000316605.5:p.His183Pro
NM_019098.4:c.548A>C NP_061971.3:p.His183Pro
XM_011517138.1:c.134A>C XP_011515440.1:p.His45Pro
XM_011517138.2:c.134A>C XP_011515440.1:p.His45Pro
NM_019098.5:c.548A>C MANE Select NP_061971.3:p.His183Pro