Canonical Allele Identifier: CA2374748969

Gene: CHRNA4

Linked Data

• dbSNP Id: rs367917715
• gnomAD v4: 20-63359542-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63359542A>C , CM000682.2:g.63359542A>C	GRCh38
NC_000020.10:g.61990894A>C , CM000682.1:g.61990894A>C	GRCh37
NC_000020.9:g.61461338A>C	NCBI36
NG_011931.1:g.6802T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.228+6T>G MANE Select	ENSP00000359285.4:n.228+6T>G
ENST00000636481.1:n.36+6T>G
ENST00000636726.1:n.33+6T>G
ENST00000675470.1:c.228+6T>G	ENSP00000502096.1:n.228+6T>G
ENST00000370263.8:c.228+6T>G	ENSP00000359285.4:n.228+6T>G
ENST00000463705.5:n.1032-8515T>G
ENST00000467563.3:n.280+6T>G
ENST00000498043.6:c.152+6T>G
ENST00000615287.4:c.-86+6T>G	ENSP00000483388.1:n.-86+6T>G
ENST00000626188.1:n.298T>G
ENST00000627000.1:c.228+6T>G	ENSP00000486914.1:n.228+6T>G
ENST00000628665.1:n.253+6T>G
NM_000744.6:c.228+6T>G	NP_000735.1:n.228+6T>G
NM_001256573.1:c.-319+6T>G	NP_001243502.1:n.-319+6T>G
NR_046317.1:n.459+6T>G
XM_017027625.2:c.-319+6T>G	XP_016883114.1:n.-319+6T>G
NM_001256573.2:c.-319+6T>G	NP_001243502.1:n.-319+6T>G
NR_046317.2:n.412+6T>G
NM_000744.7:c.228+6T>G MANE Select	NP_000735.1:n.228+6T>G