Canonical Allele Identifier: CA370808956

Gene: CHRNA2

Linked Data

• ClinVar Variation Id: 1299111
• ClinVar RCV Id: RCV001727441
• dbSNP Id: rs2132650731
• MyVariant Identifiers: chr8:g.27320666A>C (hg19) ; chr8:g.27463149A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463149A>C , CM000670.2:g.27463149A>C	GRCh38
NC_000008.10:g.27320666A>C , CM000670.1:g.27320666A>C	GRCh37
NC_000008.9:g.27376583A>C	NCBI36
NG_015827.1:g.21148T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1294T>G MANE Select	ENSP00000385026.1:p.Ser432Ala
ENST00000240132.7:c.1249T>G	ENSP00000240132.2:p.Ser417Ala
ENST00000407991.2:c.1294T>G	ENSP00000385026.1:p.Ser432Ala
ENST00000520600.1:n.290-1395T>G
ENST00000520933.7:c.1228T>G	ENSP00000429616.2:p.Ser410Ala
ENST00000523695.5:c.*696T>G	ENSP00000430612.1:n.*696T>G
NM_000742.3:c.1294T>G	NP_000733.2:p.Ser432Ala
NM_001282455.1:c.1249T>G	NP_001269384.1:p.Ser417Ala
XM_005273397.1:c.817T>G	XP_005273454.1:p.Ser273Ala
XM_006716282.1:c.1294T>G	XP_006716345.1:p.Ser432Ala
XM_011544388.1:c.1294T>G	XP_011542690.1:p.Ser432Ala
XM_011544389.1:c.700T>G	XP_011542691.1:p.Ser234Ala
NM_001347705.1:c.817T>G	NP_001334634.1:p.Ser273Ala
NM_001347706.1:c.817T>G	NP_001334635.1:p.Ser273Ala
NM_001347707.1:c.700T>G	NP_001334636.1:p.Ser234Ala
NM_001347708.1:c.700T>G	NP_001334637.1:p.Ser234Ala
XM_011544389.2:c.700T>G	XP_011542691.1:p.Ser234Ala
NM_000742.4:c.1294T>G MANE Select	NP_000733.2:p.Ser432Ala
NM_001282455.2:c.1249T>G	NP_001269384.1:p.Ser417Ala
NM_001347705.2:c.817T>G	NP_001334634.1:p.Ser273Ala
NM_001347706.2:c.817T>G	NP_001334635.1:p.Ser273Ala
NM_001347707.2:c.700T>G	NP_001334636.1:p.Ser234Ala
NM_001347708.2:c.700T>G	NP_001334637.1:p.Ser234Ala