Canonical Allele Identifier: CA371446306
Gene: CNGB3 HGNC NCBI

Linked Data

gnomAD v4: 8-86575974-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.86575974G>A , CM000670.2:g.86575974G>A GRCh38
NC_000008.10:g.87588202G>A , CM000670.1:g.87588202G>A GRCh37
NC_000008.9:g.87657318G>A NCBI36
NG_016980.1:g.172702C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000320005.6:c.2260C>T MANE Select ENSP00000316605.5:p.Pro754Ser
ENST00000681546.1:n.2080C>T
ENST00000681746.1:c.*671C>T ENSP00000505959.1:n.*671C>T
ENST00000320005.5:c.2260C>T ENSP00000316605.5:p.Pro754Ser
ENST00000517327.5:c.276+2715C>T ENSP00000428329.1:n.276+2715C>T
NM_019098.4:c.2260C>T NP_061971.3:p.Pro754Ser
XM_011517138.1:c.1846C>T XP_011515440.1:p.Pro616Ser
XM_011517138.2:c.1846C>T XP_011515440.1:p.Pro616Ser
NM_019098.5:c.2260C>T MANE Select NP_061971.3:p.Pro754Ser