Canonical Allele Identifier: CA4799742

Gene: CNGB3

Linked Data

• ClinVar Variation Id: 909568
• ClinVar RCV Id: RCV001160704 ; RCV001160705
• dbSNP Id: rs750535143
• ExAC: 8:87588112 G / A
• gnomAD v2: 8-87588112-G-A
• gnomAD v3: 8-86575884-G-A
• gnomAD v4: 8-86575884-G-A
• MyVariant Identifiers: chr8:g.87588112G>A (hg19) ; chr8:g.86575884G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86575884G>A , CM000670.2:g.86575884G>A	GRCh38
NC_000008.10:g.87588112G>A , CM000670.1:g.87588112G>A	GRCh37
NC_000008.9:g.87657228G>A	NCBI36
NG_016980.1:g.172792C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000320005.6:c.2350C>T MANE Select	ENSP00000316605.5:p.Leu784Phe
ENST00000681546.1:n.2170C>T
ENST00000681746.1:c.*761C>T	ENSP00000505959.1:n.*761C>T
ENST00000320005.5:c.2350C>T	ENSP00000316605.5:p.Leu784Phe
ENST00000517327.5:c.276+2805C>T	ENSP00000428329.1:n.276+2805C>T
NM_019098.4:c.2350C>T	NP_061971.3:p.Leu784Phe
XM_011517138.1:c.1936C>T	XP_011515440.1:p.Leu646Phe
XM_011517138.2:c.1936C>T	XP_011515440.1:p.Leu646Phe
NM_019098.5:c.2350C>T MANE Select	NP_061971.3:p.Leu784Phe