Canonical Allele Identifier: CA371448289
Gene: CNGB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647872T>G , CM000670.2:g.86647872T>G GRCh38
NC_000008.10:g.87660100T>G , CM000670.1:g.87660100T>G GRCh37
NC_000008.9:g.87729216T>G NCBI36
NG_016980.1:g.100804A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.919A>C MANE Select ENSP00000316605.5:p.Ile307Leu
ENST00000681546.1:n.739A>C
ENST00000681746.1:c.919A>C ENSP00000505959.1:p.Ile307Leu
ENST00000320005.5:c.919A>C ENSP00000316605.5:p.Ile307Leu
NM_019098.4:c.919A>C NP_061971.3:p.Ile307Leu
XM_011517138.1:c.505A>C XP_011515440.1:p.Ile169Leu
XM_011517138.2:c.505A>C XP_011515440.1:p.Ile169Leu
NM_019098.5:c.919A>C MANE Select NP_061971.3:p.Ile307Leu