Canonical Allele Identifier: CA409635591

Gene: CHRNA4

Linked Data

• dbSNP Id: rs1253642417
• MyVariant Identifiers: chr20:g.61981749G>T (hg19) ; chr20:g.63350397G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350397G>T , CM000682.2:g.63350397G>T	GRCh38
NC_000020.10:g.61981749G>T , CM000682.1:g.61981749G>T	GRCh37
NC_000020.9:g.61452193G>T	NCBI36
NG_011931.1:g.15947C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1014C>A MANE Select	ENSP00000359285.4:p.His338Gln
ENST00000370263.8:c.1014C>A	ENSP00000359285.4:p.His338Gln
ENST00000463705.5:n.1662C>A
ENST00000467563.3:n.1084C>A
ENST00000498043.6:c.1038C>A
ENST00000615287.4:c.801C>A	ENSP00000483388.1:p.His267Gln
ENST00000627000.1:c.*703C>A	ENSP00000486914.1:n.*703C>A
ENST00000630240.1:n.735C>A
NM_000744.6:c.1014C>A	NP_000735.1:p.His338Gln
NM_001256573.1:c.486C>A	NP_001243502.1:p.His162Gln
NR_046317.1:n.1270C>A
XM_011528524.1:c.801C>A	XP_011526826.1:p.His267Gln
XM_017027625.2:c.486C>A	XP_016883114.1:p.His162Gln
XM_024451822.1:c.486C>A	XP_024307590.1:p.His162Gln
NM_001256573.2:c.486C>A	NP_001243502.1:p.His162Gln
NR_046317.2:n.1223C>A
NM_000744.7:c.1014C>A MANE Select	NP_000735.1:p.His338Gln