Canonical Allele Identifier: CA409635711

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981769G>A (hg19) ; chr20:g.63350417G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350417G>A , CM000682.2:g.63350417G>A	GRCh38
NC_000020.10:g.61981769G>A , CM000682.1:g.61981769G>A	GRCh37
NC_000020.9:g.61452213G>A	NCBI36
NG_011931.1:g.15927C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.994C>T MANE Select	ENSP00000359285.4:p.His332Tyr
ENST00000370263.8:c.994C>T	ENSP00000359285.4:p.His332Tyr
ENST00000463705.5:n.1642C>T
ENST00000467563.3:n.1064C>T
ENST00000498043.6:c.1018C>T
ENST00000615287.4:c.781C>T	ENSP00000483388.1:p.His261Tyr
ENST00000627000.1:c.*683C>T	ENSP00000486914.1:n.*683C>T
ENST00000630240.1:n.715C>T
NM_000744.6:c.994C>T	NP_000735.1:p.His332Tyr
NM_001256573.1:c.466C>T	NP_001243502.1:p.His156Tyr
NR_046317.1:n.1250C>T
XM_011528524.1:c.781C>T	XP_011526826.1:p.His261Tyr
XM_017027625.2:c.466C>T	XP_016883114.1:p.His156Tyr
XM_024451822.1:c.466C>T	XP_024307590.1:p.His156Tyr
NM_001256573.2:c.466C>T	NP_001243502.1:p.His156Tyr
NR_046317.2:n.1203C>T
NM_000744.7:c.994C>T MANE Select	NP_000735.1:p.His332Tyr