Canonical Allele Identifier: CA371448301
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86647880-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86647880A>G , CM000670.2:g.86647880A>G GRCh38
NC_000008.10:g.87660108A>G , CM000670.1:g.87660108A>G GRCh37
NC_000008.9:g.87729224A>G NCBI36
NG_016980.1:g.100796T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.911T>C MANE Select ENSP00000316605.5:p.Val304Ala
ENST00000681546.1:n.731T>C
ENST00000681746.1:c.911T>C ENSP00000505959.1:p.Val304Ala
ENST00000320005.5:c.911T>C ENSP00000316605.5:p.Val304Ala
NM_019098.4:c.911T>C NP_061971.3:p.Val304Ala
XM_011517138.1:c.497T>C XP_011515440.1:p.Val166Ala
XM_011517138.2:c.497T>C XP_011515440.1:p.Val166Ala
NM_019098.5:c.911T>C MANE Select NP_061971.3:p.Val304Ala