Canonical Allele Identifier: CA409636357

Gene: CHRNA4

Linked Data

• dbSNP Id: rs2068577450
• gnomAD v3: 20-63350525-T-C
• gnomAD v4: 20-63350525-T-C
• MyVariant Identifiers: chr20:g.61981877T>C (hg19) ; chr20:g.63350525T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350525T>C , CM000682.2:g.63350525T>C	GRCh38
NC_000020.10:g.61981877T>C , CM000682.1:g.61981877T>C	GRCh37
NC_000020.9:g.61452321T>C	NCBI36
NG_011931.1:g.15819A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.886A>G MANE Select	ENSP00000359285.4:p.Ile296Val
ENST00000370263.8:c.886A>G	ENSP00000359285.4:p.Ile296Val
ENST00000463705.5:n.1534A>G
ENST00000467563.3:n.956A>G
ENST00000498043.6:c.910A>G
ENST00000615287.4:c.673A>G	ENSP00000483388.1:p.Ile225Val
ENST00000627000.1:c.*575A>G	ENSP00000486914.1:n.*575A>G
ENST00000630240.1:n.607A>G
NM_000744.6:c.886A>G	NP_000735.1:p.Ile296Val
NM_001256573.1:c.358A>G	NP_001243502.1:p.Ile120Val
NR_046317.1:n.1142A>G
XM_011528524.1:c.673A>G	XP_011526826.1:p.Ile225Val
XM_017027625.2:c.358A>G	XP_016883114.1:p.Ile120Val
XM_024451822.1:c.358A>G	XP_024307590.1:p.Ile120Val
NM_001256573.2:c.358A>G	NP_001243502.1:p.Ile120Val
NR_046317.2:n.1095A>G
NM_000744.7:c.886A>G MANE Select	NP_000735.1:p.Ile296Val