Canonical Allele Identifier: CA409637356

Gene: CHRNA4

Linked Data

• dbSNP Id: rs2068584053
• gnomAD v3: 20-63350765-C-T
• gnomAD v4: 20-63350765-C-T
• MyVariant Identifiers: chr20:g.61982117C>T (hg19) ; chr20:g.63350765C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350765C>T , CM000682.2:g.63350765C>T	GRCh38
NC_000020.10:g.61982117C>T , CM000682.1:g.61982117C>T	GRCh37
NC_000020.9:g.61452561C>T	NCBI36
NG_011931.1:g.15579G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.646G>A MANE Select	ENSP00000359285.4:p.Gly216Ser
ENST00000370263.8:c.646G>A	ENSP00000359285.4:p.Gly216Ser
ENST00000463705.5:n.1294G>A
ENST00000467563.3:n.716G>A
ENST00000498043.6:c.670G>A
ENST00000615287.4:c.433G>A	ENSP00000483388.1:p.Gly145Ser
ENST00000627000.1:c.*335G>A	ENSP00000486914.1:n.*335G>A
ENST00000630240.1:n.367G>A
NM_000744.6:c.646G>A	NP_000735.1:p.Gly216Ser
NM_001256573.1:c.118G>A	NP_001243502.1:p.Gly40Ser
NR_046317.1:n.902G>A
XM_011528524.1:c.433G>A	XP_011526826.1:p.Gly145Ser
XM_017027625.2:c.118G>A	XP_016883114.1:p.Gly40Ser
XM_024451822.1:c.118G>A	XP_024307590.1:p.Gly40Ser
NM_001256573.2:c.118G>A	NP_001243502.1:p.Gly40Ser
NR_046317.2:n.855G>A
NM_000744.7:c.646G>A MANE Select	NP_000735.1:p.Gly216Ser