Canonical Allele Identifier: CA317435777

Gene: CHRNA4

Linked Data

• dbSNP Id: rs1035741624
• MyVariant Identifiers: chr20:g.61981949C>T (hg19) ; chr20:g.63350597C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350597C>T , CM000682.2:g.63350597C>T	GRCh38
NC_000020.10:g.61981949C>T , CM000682.1:g.61981949C>T	GRCh37
NC_000020.9:g.61452393C>T	NCBI36
NG_011931.1:g.15747G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.814G>A MANE Select	ENSP00000359285.4:p.Gly272Ser
ENST00000370263.8:c.814G>A	ENSP00000359285.4:p.Gly272Ser
ENST00000463705.5:n.1462G>A
ENST00000467563.3:n.884G>A
ENST00000498043.6:c.838G>A
ENST00000615287.4:c.601G>A	ENSP00000483388.1:p.Gly201Ser
ENST00000627000.1:c.*503G>A	ENSP00000486914.1:n.*503G>A
ENST00000630240.1:n.535G>A
NM_000744.6:c.814G>A	NP_000735.1:p.Gly272Ser
NM_001256573.1:c.286G>A	NP_001243502.1:p.Gly96Ser
NR_046317.1:n.1070G>A
XM_011528524.1:c.601G>A	XP_011526826.1:p.Gly201Ser
XM_017027625.2:c.286G>A	XP_016883114.1:p.Gly96Ser
XM_024451822.1:c.286G>A	XP_024307590.1:p.Gly96Ser
NM_001256573.2:c.286G>A	NP_001243502.1:p.Gly96Ser
NR_046317.2:n.1023G>A
NM_000744.7:c.814G>A MANE Select	NP_000735.1:p.Gly272Ser