Canonical Allele Identifier: CA2687826684

Gene: CNGB3

Linked Data

• gnomAD v4: 8-86671132-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86671132C>A , CM000670.2:g.86671132C>A	GRCh38
NC_000008.10:g.87683360C>A , CM000670.1:g.87683360C>A	GRCh37
NC_000008.9:g.87752476C>A	NCBI36
NG_016980.1:g.77544G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.339-34G>T MANE Select	ENSP00000316605.5:n.339-34G>T
ENST00000680314.1:n.100-34G>T
ENST00000681746.1:c.339-34G>T	ENSP00000505959.1:n.339-34G>T
ENST00000320005.5:c.339-34G>T	ENSP00000316605.5:n.339-34G>T
NM_019098.4:c.339-34G>T	NP_061971.3:n.339-34G>T
XM_011517138.1:c.-76-34G>T	XP_011515440.1:n.-76-34G>T
XM_011517138.2:c.-76-34G>T	XP_011515440.1:n.-76-34G>T
NM_019098.5:c.339-34G>T MANE Select	NP_061971.3:n.339-34G>T