Canonical Allele Identifier: CA511338735

Gene: CHRNA4

Linked Data

• dbSNP Id: rs2123471838
• MyVariant Identifiers: chr20:g.61981764G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350412G>A , CM000682.2:g.63350412G>A	GRCh38
NC_000020.10:g.61981764G>A , CM000682.1:g.61981764G>A	GRCh37
NC_000020.9:g.61452208G>A	NCBI36
NG_011931.1:g.15932C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.999C>T MANE Select	ENSP00000359285.4:p.Arg333=
ENST00000370263.8:c.999C>T	ENSP00000359285.4:p.Arg333=
ENST00000463705.5:n.1647C>T
ENST00000467563.3:n.1069C>T
ENST00000498043.6:c.1023C>T
ENST00000615287.4:c.786C>T	ENSP00000483388.1:p.Arg262=
ENST00000627000.1:c.*688C>T	ENSP00000486914.1:n.*688C>T
ENST00000630240.1:n.720C>T
NM_000744.6:c.999C>T	NP_000735.1:p.Arg333=
NM_001256573.1:c.471C>T	NP_001243502.1:p.Arg157=
NR_046317.1:n.1255C>T
XM_011528524.1:c.786C>T	XP_011526826.1:p.Arg262=
XM_017027625.2:c.471C>T	XP_016883114.1:p.Arg157=
XM_024451822.1:c.471C>T	XP_024307590.1:p.Arg157=
NM_001256573.2:c.471C>T	NP_001243502.1:p.Arg157=
NR_046317.2:n.1208C>T
NM_000744.7:c.999C>T MANE Select	NP_000735.1:p.Arg333=