Canonical Allele Identifier: CA746462884

Gene: CHRNA4

Linked Data

• dbSNP Id: rs2273504
• gnomAD v3: 20-63356709-G-T
• gnomAD v4: 20-63356709-G-T
• MyVariant Identifiers: chr20:g.61988061G>T (hg19) ; chr20:g.63356709G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63356709G>T , CM000682.2:g.63356709G>T	GRCh38
NC_000020.10:g.61988061G>T , CM000682.1:g.61988061G>T	GRCh37
NC_000020.9:g.61458505G>T	NCBI36
NG_011931.1:g.9635C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.229-294C>A MANE Select	ENSP00000359285.4:n.229-294C>A
ENST00000636481.1:n.37-171C>A
ENST00000636726.1:n.34-105C>A
ENST00000675470.1:c.229-294C>A	ENSP00000502096.1:n.229-294C>A
ENST00000370263.8:c.229-294C>A	ENSP00000359285.4:n.229-294C>A
ENST00000463705.5:n.1032-5682C>A
ENST00000467563.3:n.281-294C>A
ENST00000498043.6:c.153-294C>A
ENST00000615287.4:c.-85-294C>A	ENSP00000483388.1:n.-85-294C>A
ENST00000627000.1:c.229-294C>A	ENSP00000486914.1:n.229-294C>A
ENST00000628665.1:n.254-294C>A
NM_000744.6:c.229-294C>A	NP_000735.1:n.229-294C>A
NM_001256573.1:c.-318-294C>A	NP_001243502.1:n.-318-294C>A
NR_046317.1:n.460-294C>A
XM_017027625.2:c.-318-294C>A	XP_016883114.1:n.-318-294C>A
NM_001256573.2:c.-318-294C>A	NP_001243502.1:n.-318-294C>A
NR_046317.2:n.413-294C>A
NM_000744.7:c.229-294C>A MANE Select	NP_000735.1:n.229-294C>A