Canonical Allele Identifier: CA371449892
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668111T>G , CM000670.2:g.86668111T>G GRCh38
NC_000008.10:g.87680339T>G , CM000670.1:g.87680339T>G GRCh37
NC_000008.9:g.87749455T>G NCBI36
NG_016980.1:g.80565A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.551A>C MANE Select ENSP00000316605.5:p.Tyr184Ser
ENST00000681746.1:c.551A>C ENSP00000505959.1:p.Tyr184Ser
ENST00000320005.5:c.551A>C ENSP00000316605.5:p.Tyr184Ser
NM_019098.4:c.551A>C NP_061971.3:p.Tyr184Ser
XM_011517138.1:c.137A>C XP_011515440.1:p.Tyr46Ser
XM_011517138.2:c.137A>C XP_011515440.1:p.Tyr46Ser
NM_019098.5:c.551A>C MANE Select NP_061971.3:p.Tyr184Ser