Canonical Allele Identifier: CA317435442

Gene: CHRNA4

Linked Data

• dbSNP Id: rs553885477
• gnomAD v3: 20-63350385-G-C
• gnomAD v4: 20-63350385-G-C
• MyVariant Identifiers: chr20:g.61981737G>C (hg19) ; chr20:g.63350385G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350385G>C , CM000682.2:g.63350385G>C	GRCh38
NC_000020.10:g.61981737G>C , CM000682.1:g.61981737G>C	GRCh37
NC_000020.9:g.61452181G>C	NCBI36
NG_011931.1:g.15959C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1026C>G MANE Select	ENSP00000359285.4:p.Thr342=
ENST00000370263.8:c.1026C>G	ENSP00000359285.4:p.Thr342=
ENST00000463705.5:n.1674C>G
ENST00000467563.3:n.1096C>G
ENST00000498043.6:c.1050C>G
ENST00000615287.4:c.813C>G	ENSP00000483388.1:p.Thr271=
ENST00000627000.1:c.*715C>G	ENSP00000486914.1:n.*715C>G
ENST00000630240.1:n.747C>G
NM_000744.6:c.1026C>G	NP_000735.1:p.Thr342=
NM_001256573.1:c.498C>G	NP_001243502.1:p.Thr166=
NR_046317.1:n.1282C>G
XM_011528524.1:c.813C>G	XP_011526826.1:p.Thr271=
XM_017027625.2:c.498C>G	XP_016883114.1:p.Thr166=
XM_024451822.1:c.498C>G	XP_024307590.1:p.Thr166=
NM_001256573.2:c.498C>G	NP_001243502.1:p.Thr166=
NR_046317.2:n.1235C>G
NM_000744.7:c.1026C>G MANE Select	NP_000735.1:p.Thr342=