Canonical Allele Identifier: CA511338820

Gene: CHRNA4

Linked Data

• dbSNP Id: rs1452503572
• gnomAD v2: 20-61981809-G-A
• gnomAD v4: 20-63350457-G-A
• MyVariant Identifiers: chr20:g.61981809G>A (hg19) ; chr20:g.63350457G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350457G>A , CM000682.2:g.63350457G>A	GRCh38
NC_000020.10:g.61981809G>A , CM000682.1:g.61981809G>A	GRCh37
NC_000020.9:g.61452253G>A	NCBI36
NG_011931.1:g.15887C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.954C>T MANE Select	ENSP00000359285.4:p.Thr318=
ENST00000370263.8:c.954C>T	ENSP00000359285.4:p.Thr318=
ENST00000463705.5:n.1602C>T
ENST00000467563.3:n.1024C>T
ENST00000498043.6:c.978C>T
ENST00000615287.4:c.741C>T	ENSP00000483388.1:p.Thr247=
ENST00000627000.1:c.*643C>T	ENSP00000486914.1:n.*643C>T
ENST00000630240.1:n.675C>T
NM_000744.6:c.954C>T	NP_000735.1:p.Thr318=
NM_001256573.1:c.426C>T	NP_001243502.1:p.Thr142=
NR_046317.1:n.1210C>T
XM_011528524.1:c.741C>T	XP_011526826.1:p.Thr247=
XM_017027625.2:c.426C>T	XP_016883114.1:p.Thr142=
XM_024451822.1:c.426C>T	XP_024307590.1:p.Thr142=
NM_001256573.2:c.426C>T	NP_001243502.1:p.Thr142=
NR_046317.2:n.1163C>T
NM_000744.7:c.954C>T MANE Select	NP_000735.1:p.Thr318=