Canonical Allele Identifier: CA371447953
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579202T>A , CM000670.2:g.86579202T>A GRCh38
NC_000008.10:g.87591430T>A , CM000670.1:g.87591430T>A GRCh37
NC_000008.9:g.87660546T>A NCBI36
NG_016980.1:g.169474A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1832A>T MANE Select ENSP00000316605.5:p.His611Leu
ENST00000681546.1:n.1652A>T
ENST00000681746.1:c.*243A>T ENSP00000505959.1:n.*243A>T
ENST00000320005.5:c.1832A>T ENSP00000316605.5:p.His611Leu
ENST00000517327.5:c.5A>T ENSP00000428329.1:p.His2Leu
NM_019098.4:c.1832A>T NP_061971.3:p.His611Leu
XM_011517138.1:c.1418A>T XP_011515440.1:p.His473Leu
XM_011517138.2:c.1418A>T XP_011515440.1:p.His473Leu
NM_019098.5:c.1832A>T MANE Select NP_061971.3:p.His611Leu