Canonical Allele Identifier: CA370809278

Gene: CHRNA2

Linked Data

• ClinVar Variation Id: 1524032
• ClinVar RCV Id: RCV002031419
• dbSNP Id: rs762406891
• MyVariant Identifiers: chr8:g.27320786G>C (hg19) ; chr8:g.27463269G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.27463269G>C , CM000670.2:g.27463269G>C	GRCh38
NC_000008.10:g.27320786G>C , CM000670.1:g.27320786G>C	GRCh37
NC_000008.9:g.27376703G>C	NCBI36
NG_015827.1:g.21028C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407991.3:c.1174C>G MANE Select	ENSP00000385026.1:p.Pro392Ala
ENST00000240132.7:c.1129C>G	ENSP00000240132.2:p.Pro377Ala
ENST00000407991.2:c.1174C>G	ENSP00000385026.1:p.Pro392Ala
ENST00000520600.1:n.290-1515C>G
ENST00000520933.7:c.1108C>G	ENSP00000429616.2:p.Pro370Ala
ENST00000523695.5:c.*576C>G	ENSP00000430612.1:n.*576C>G
NM_000742.3:c.1174C>G	NP_000733.2:p.Pro392Ala
NM_001282455.1:c.1129C>G	NP_001269384.1:p.Pro377Ala
XM_005273397.1:c.697C>G	XP_005273454.1:p.Pro233Ala
XM_006716282.1:c.1174C>G	XP_006716345.1:p.Pro392Ala
XM_011544388.1:c.1174C>G	XP_011542690.1:p.Pro392Ala
XM_011544389.1:c.580C>G	XP_011542691.1:p.Pro194Ala
NM_001347705.1:c.697C>G	NP_001334634.1:p.Pro233Ala
NM_001347706.1:c.697C>G	NP_001334635.1:p.Pro233Ala
NM_001347707.1:c.580C>G	NP_001334636.1:p.Pro194Ala
NM_001347708.1:c.580C>G	NP_001334637.1:p.Pro194Ala
XM_011544389.2:c.580C>G	XP_011542691.1:p.Pro194Ala
NM_000742.4:c.1174C>G MANE Select	NP_000733.2:p.Pro392Ala
NM_001282455.2:c.1129C>G	NP_001269384.1:p.Pro377Ala
NM_001347705.2:c.697C>G	NP_001334634.1:p.Pro233Ala
NM_001347706.2:c.697C>G	NP_001334635.1:p.Pro233Ala
NM_001347707.2:c.580C>G	NP_001334636.1:p.Pro194Ala
NM_001347708.2:c.580C>G	NP_001334637.1:p.Pro194Ala