Canonical Allele Identifier: CA409638350

Gene: CHRNA4

Linked Data

• ClinVar Variation Id: 634555
• ClinVar RCV Id: RCV000785066
• dbSNP Id: rs1568810867
• MyVariant Identifiers: chr20:g.61982267T>A (hg19) ; chr20:g.63350915T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350915T>A , CM000682.2:g.63350915T>A	GRCh38
NC_000020.10:g.61982267T>A , CM000682.1:g.61982267T>A	GRCh37
NC_000020.9:g.61452711T>A	NCBI36
NG_011931.1:g.15429A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.496A>T MANE Select	ENSP00000359285.4:p.Thr166Ser
ENST00000370263.8:c.496A>T	ENSP00000359285.4:p.Thr166Ser
ENST00000463705.5:n.1144A>T
ENST00000467563.3:n.566A>T
ENST00000498043.6:c.520A>T
ENST00000615287.4:c.283A>T	ENSP00000483388.1:p.Thr95Ser
ENST00000627000.1:c.*185A>T	ENSP00000486914.1:n.*185A>T
ENST00000628665.1:n.539A>T
ENST00000630240.1:n.217A>T
NM_000744.6:c.496A>T	NP_000735.1:p.Thr166Ser
NM_001256573.1:c.-33A>T	NP_001243502.1:n.-33A>T
NR_046317.1:n.752A>T
XM_011528524.1:c.283A>T	XP_011526826.1:p.Thr95Ser
XM_017027625.2:c.-33A>T	XP_016883114.1:n.-33A>T
XM_024451822.1:c.-33A>T	XP_024307590.1:n.-33A>T
NM_001256573.2:c.-33A>T	NP_001243502.1:n.-33A>T
NR_046317.2:n.705A>T
NM_000744.7:c.496A>T MANE Select	NP_000735.1:p.Thr166Ser