Canonical Allele Identifier: CA371449879
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86668106-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86668106T>A , CM000670.2:g.86668106T>A GRCh38
NC_000008.10:g.87680334T>A , CM000670.1:g.87680334T>A GRCh37
NC_000008.9:g.87749450T>A NCBI36
NG_016980.1:g.80570A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.556A>T MANE Select ENSP00000316605.5:p.Arg186Trp
ENST00000681746.1:c.556A>T ENSP00000505959.1:p.Arg186Trp
ENST00000320005.5:c.556A>T ENSP00000316605.5:p.Arg186Trp
NM_019098.4:c.556A>T NP_061971.3:p.Arg186Trp
XM_011517138.1:c.142A>T XP_011515440.1:p.Arg48Trp
XM_011517138.2:c.142A>T XP_011515440.1:p.Arg48Trp
NM_019098.5:c.556A>T MANE Select NP_061971.3:p.Arg186Trp