Canonical Allele Identifier: CA409635608

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981751G>A (hg19) ; chr20:g.63350399G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350399G>A , CM000682.2:g.63350399G>A	GRCh38
NC_000020.10:g.61981751G>A , CM000682.1:g.61981751G>A	GRCh37
NC_000020.9:g.61452195G>A	NCBI36
NG_011931.1:g.15945C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1012C>T MANE Select	ENSP00000359285.4:p.His338Tyr
ENST00000370263.8:c.1012C>T	ENSP00000359285.4:p.His338Tyr
ENST00000463705.5:n.1660C>T
ENST00000467563.3:n.1082C>T
ENST00000498043.6:c.1036C>T
ENST00000615287.4:c.799C>T	ENSP00000483388.1:p.His267Tyr
ENST00000627000.1:c.*701C>T	ENSP00000486914.1:n.*701C>T
ENST00000630240.1:n.733C>T
NM_000744.6:c.1012C>T	NP_000735.1:p.His338Tyr
NM_001256573.1:c.484C>T	NP_001243502.1:p.His162Tyr
NR_046317.1:n.1268C>T
XM_011528524.1:c.799C>T	XP_011526826.1:p.His267Tyr
XM_017027625.2:c.484C>T	XP_016883114.1:p.His162Tyr
XM_024451822.1:c.484C>T	XP_024307590.1:p.His162Tyr
NM_001256573.2:c.484C>T	NP_001243502.1:p.His162Tyr
NR_046317.2:n.1221C>T
NM_000744.7:c.1012C>T MANE Select	NP_000735.1:p.His338Tyr