Canonical Allele Identifier: CA461813774

Gene: CNGB3

Linked Data

• MyVariant Identifiers: chr8:g.87645013A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.86632785A>C , CM000670.2:g.86632785A>C	GRCh38
NC_000008.10:g.87645013A>C , CM000670.1:g.87645013A>C	GRCh37
NC_000008.9:g.87714129A>C	NCBI36
NG_016980.1:g.115891T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320005.6:c.1287T>G MANE Select	ENSP00000316605.5:p.Ser429=
ENST00000681546.1:n.1107T>G
ENST00000681746.1:c.1287T>G	ENSP00000505959.1:p.Ser429=
ENST00000320005.5:c.1287T>G	ENSP00000316605.5:p.Ser429=
NM_019098.4:c.1287T>G	NP_061971.3:p.Ser429=
XM_011517138.1:c.873T>G	XP_011515440.1:p.Ser291=
XM_011517138.2:c.873T>G	XP_011515440.1:p.Ser291=
NM_019098.5:c.1287T>G MANE Select	NP_061971.3:p.Ser429=