Canonical Allele Identifier: CA317436373

Gene: CHRNA4

Linked Data

• dbSNP Id: rs61734382
• MyVariant Identifiers: chr20:g.61982274G>C (hg19) ; chr20:g.63350922G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350922G>C , CM000682.2:g.63350922G>C	GRCh38
NC_000020.10:g.61982274G>C , CM000682.1:g.61982274G>C	GRCh37
NC_000020.9:g.61452718G>C	NCBI36
NG_011931.1:g.15422C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.489C>G MANE Select	ENSP00000359285.4:p.Ile163Met
ENST00000370263.8:c.489C>G	ENSP00000359285.4:p.Ile163Met
ENST00000463705.5:n.1137C>G
ENST00000467563.3:n.559C>G
ENST00000498043.6:c.513C>G
ENST00000615287.4:c.276C>G	ENSP00000483388.1:p.Ile92Met
ENST00000627000.1:c.*178C>G	ENSP00000486914.1:n.*178C>G
ENST00000628665.1:n.532C>G
ENST00000630240.1:n.210C>G
NM_000744.6:c.489C>G	NP_000735.1:p.Ile163Met
NM_001256573.1:c.-40C>G	NP_001243502.1:n.-40C>G
NR_046317.1:n.745C>G
XM_011528524.1:c.276C>G	XP_011526826.1:p.Ile92Met
XM_017027625.2:c.-40C>G	XP_016883114.1:n.-40C>G
XM_024451822.1:c.-40C>G	XP_024307590.1:n.-40C>G
NM_001256573.2:c.-40C>G	NP_001243502.1:n.-40C>G
NR_046317.2:n.698C>G
NM_000744.7:c.489C>G MANE Select	NP_000735.1:p.Ile163Met