Canonical Allele Identifier: CA370808997

Gene: CHRNA2

Linked Data

• ClinVar Variation Id: 1018032
• ClinVar RCV Id: RCV001317273
• dbSNP Id: rs1179640861
• gnomAD v4: 8-27463170-A-G
• MyVariant Identifiers: chr8:g.27320687A>G (hg19) ; chr8:g.27463170A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463170A>G , CM000670.2:g.27463170A>G	GRCh38
NC_000008.10:g.27320687A>G , CM000670.1:g.27320687A>G	GRCh37
NC_000008.9:g.27376604A>G	NCBI36
NG_015827.1:g.21127T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1273T>C MANE Select	ENSP00000385026.1:p.Cys425Arg
ENST00000240132.7:c.1228T>C	ENSP00000240132.2:p.Cys410Arg
ENST00000407991.2:c.1273T>C	ENSP00000385026.1:p.Cys425Arg
ENST00000520600.1:n.290-1416T>C
ENST00000520933.7:c.1207T>C	ENSP00000429616.2:p.Cys403Arg
ENST00000523695.5:c.*675T>C	ENSP00000430612.1:n.*675T>C
NM_000742.3:c.1273T>C	NP_000733.2:p.Cys425Arg
NM_001282455.1:c.1228T>C	NP_001269384.1:p.Cys410Arg
XM_005273397.1:c.796T>C	XP_005273454.1:p.Cys266Arg
XM_006716282.1:c.1273T>C	XP_006716345.1:p.Cys425Arg
XM_011544388.1:c.1273T>C	XP_011542690.1:p.Cys425Arg
XM_011544389.1:c.679T>C	XP_011542691.1:p.Cys227Arg
NM_001347705.1:c.796T>C	NP_001334634.1:p.Cys266Arg
NM_001347706.1:c.796T>C	NP_001334635.1:p.Cys266Arg
NM_001347707.1:c.679T>C	NP_001334636.1:p.Cys227Arg
NM_001347708.1:c.679T>C	NP_001334637.1:p.Cys227Arg
XM_011544389.2:c.679T>C	XP_011542691.1:p.Cys227Arg
NM_000742.4:c.1273T>C MANE Select	NP_000733.2:p.Cys425Arg
NM_001282455.2:c.1228T>C	NP_001269384.1:p.Cys410Arg
NM_001347705.2:c.796T>C	NP_001334634.1:p.Cys266Arg
NM_001347706.2:c.796T>C	NP_001334635.1:p.Cys266Arg
NM_001347707.2:c.679T>C	NP_001334636.1:p.Cys227Arg
NM_001347708.2:c.679T>C	NP_001334637.1:p.Cys227Arg