Canonical Allele Identifier: CA409634455

Gene: CHRNA4

Linked Data

• dbSNP Id: rs2068569841
• gnomAD v4: 20-63350288-T-C
• MyVariant Identifiers: chr20:g.61981640T>C (hg19) ; chr20:g.63350288T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350288T>C , CM000682.2:g.63350288T>C	GRCh38
NC_000020.10:g.61981640T>C , CM000682.1:g.61981640T>C	GRCh37
NC_000020.9:g.61452084T>C	NCBI36
NG_011931.1:g.16056A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1123A>G MANE Select	ENSP00000359285.4:p.Met375Val
ENST00000370263.8:c.1123A>G	ENSP00000359285.4:p.Met375Val
ENST00000463705.5:n.1771A>G
ENST00000467563.3:n.1193A>G
ENST00000498043.6:c.1147A>G
ENST00000615287.4:c.910A>G	ENSP00000483388.1:p.Met304Val
ENST00000627000.1:c.*812A>G	ENSP00000486914.1:n.*812A>G
ENST00000630240.1:n.844A>G
NM_000744.6:c.1123A>G	NP_000735.1:p.Met375Val
NM_001256573.1:c.595A>G	NP_001243502.1:p.Met199Val
NR_046317.1:n.1379A>G
XM_011528524.1:c.910A>G	XP_011526826.1:p.Met304Val
XM_017027625.2:c.595A>G	XP_016883114.1:p.Met199Val
XM_024451822.1:c.595A>G	XP_024307590.1:p.Met199Val
NM_001256573.2:c.595A>G	NP_001243502.1:p.Met199Val
NR_046317.2:n.1332A>G
NM_000744.7:c.1123A>G MANE Select	NP_000735.1:p.Met375Val