Canonical Allele Identifier: CA371447968
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86579209C>G , CM000670.2:g.86579209C>G GRCh38
NC_000008.10:g.87591437C>G , CM000670.1:g.87591437C>G GRCh37
NC_000008.9:g.87660553C>G NCBI36
NG_016980.1:g.169467G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.1825G>C MANE Select ENSP00000316605.5:p.Val609Leu
ENST00000681546.1:n.1645G>C
ENST00000681746.1:c.*236G>C ENSP00000505959.1:n.*236G>C
ENST00000320005.5:c.1825G>C ENSP00000316605.5:p.Val609Leu
NM_019098.4:c.1825G>C NP_061971.3:p.Val609Leu
XM_011517138.1:c.1411G>C XP_011515440.1:p.Val471Leu
XM_011517138.2:c.1411G>C XP_011515440.1:p.Val471Leu
NM_019098.5:c.1825G>C MANE Select NP_061971.3:p.Val609Leu