Canonical Allele Identifier: CA370810794

Gene: CHRNA2

Linked Data

• dbSNP Id: rs201370407
• gnomAD v4: 8-27463680-C-A
• COSMIC: COSM6325871
• MyVariant Identifiers: chr8:g.27321197C>A (hg19) ; chr8:g.27463680C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463680C>A , CM000670.2:g.27463680C>A	GRCh38
NC_000008.10:g.27321197C>A , CM000670.1:g.27321197C>A	GRCh37
NC_000008.9:g.27377114C>A	NCBI36
NG_015827.1:g.20617G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000407991.3:c.763G>T MANE Select	ENSP00000385026.1:p.Val255Phe
ENST00000637241.1:c.*593G>T	ENSP00000490690.1:n.*593G>T
ENST00000240132.7:c.718G>T	ENSP00000240132.2:p.Val240Phe
ENST00000407991.2:c.763G>T	ENSP00000385026.1:p.Val255Phe
ENST00000520600.1:n.290-1926G>T
ENST00000520933.7:c.697G>T	ENSP00000429616.2:p.Val233Phe
ENST00000522008.1:n.493G>T
ENST00000523695.5:c.*165G>T	ENSP00000430612.1:n.*165G>T
NM_000742.3:c.763G>T	NP_000733.2:p.Val255Phe
NM_001282455.1:c.718G>T	NP_001269384.1:p.Val240Phe
XM_005273397.1:c.286G>T	XP_005273454.1:p.Val96Phe
XM_006716282.1:c.763G>T	XP_006716345.1:p.Val255Phe
XM_011544388.1:c.763G>T	XP_011542690.1:p.Val255Phe
XM_011544389.1:c.169G>T	XP_011542691.1:p.Val57Phe
NM_001347705.1:c.286G>T	NP_001334634.1:p.Val96Phe
NM_001347706.1:c.286G>T	NP_001334635.1:p.Val96Phe
NM_001347707.1:c.169G>T	NP_001334636.1:p.Val57Phe
NM_001347708.1:c.169G>T	NP_001334637.1:p.Val57Phe
XM_011544389.2:c.169G>T	XP_011542691.1:p.Val57Phe
NM_000742.4:c.763G>T MANE Select	NP_000733.2:p.Val255Phe
NM_001282455.2:c.718G>T	NP_001269384.1:p.Val240Phe
NM_001347705.2:c.286G>T	NP_001334634.1:p.Val96Phe
NM_001347706.2:c.286G>T	NP_001334635.1:p.Val96Phe
NM_001347707.2:c.169G>T	NP_001334636.1:p.Val57Phe
NM_001347708.2:c.169G>T	NP_001334637.1:p.Val57Phe