Canonical Allele Identifier: CA371444144

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87645024T>C (hg19) ; chr8:g.86632796T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86632796T>C , CM000670.2:g.86632796T>C	GRCh38
NC_000008.10:g.87645024T>C , CM000670.1:g.87645024T>C	GRCh37
NC_000008.9:g.87714140T>C	NCBI36
NG_016980.1:g.115880A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1276A>G MANE Select	ENSP00000316605.5:p.Asn426Asp
ENST00000681546.1:n.1096A>G
ENST00000681746.1:c.1276A>G	ENSP00000505959.1:p.Asn426Asp
ENST00000320005.5:c.1276A>G	ENSP00000316605.5:p.Asn426Asp
NM_019098.4:c.1276A>G	NP_061971.3:p.Asn426Asp
XM_011517138.1:c.862A>G	XP_011515440.1:p.Asn288Asp
XM_011517138.2:c.862A>G	XP_011515440.1:p.Asn288Asp
NM_019098.5:c.1276A>G MANE Select	NP_061971.3:p.Asn426Asp