Canonical Allele Identifier: CA511338439

Gene: CHRNA4

Linked Data

• dbSNP Id: rs1374296868
• gnomAD v2: 20-61981188-C-T
• gnomAD v4: 20-63349836-C-T
• MyVariant Identifiers: chr20:g.61981188C>T (hg19) ; chr20:g.63349836C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349836C>T , CM000682.2:g.63349836C>T	GRCh38
NC_000020.10:g.61981188C>T , CM000682.1:g.61981188C>T	GRCh37
NC_000020.9:g.61451632C>T	NCBI36
NG_011931.1:g.16508G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1575G>A MANE Select	ENSP00000359285.4:p.Gln525=
ENST00000370263.8:c.1575G>A	ENSP00000359285.4:p.Gln525=
ENST00000463705.5:n.2223G>A
ENST00000467563.3:n.1645G>A
ENST00000498043.6:c.1599G>A
ENST00000615287.4:c.1362G>A	ENSP00000483388.1:p.Gln454=
ENST00000627000.1:c.*1264G>A	ENSP00000486914.1:n.*1264G>A
ENST00000630240.1:n.1296G>A
NM_000744.6:c.1575G>A	NP_000735.1:p.Gln525=
NM_001256573.1:c.1047G>A	NP_001243502.1:p.Gln349=
NR_046317.1:n.1831G>A
XM_011528524.1:c.1362G>A	XP_011526826.1:p.Gln454=
XM_017027625.2:c.1047G>A	XP_016883114.1:p.Gln349=
XM_024451822.1:c.1047G>A	XP_024307590.1:p.Gln349=
NM_001256573.2:c.1047G>A	NP_001243502.1:p.Gln349=
NR_046317.2:n.1784G>A
NM_000744.7:c.1575G>A MANE Select	NP_000735.1:p.Gln525=