Canonical Allele Identifier: CA393584750

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78601857-A-C
• MyVariant Identifiers: chr15:g.78894199A>C (hg19) ; chr15:g.78601857A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601857A>C , CM000677.2:g.78601857A>C	GRCh38
NC_000015.9:g.78894199A>C , CM000677.1:g.78894199A>C	GRCh37
NC_000015.8:g.76681254A>C	NCBI36
NG_016143.1:g.24439T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.785T>G MANE Select	ENSP00000315602.5:p.Val262Gly
ENST00000326828.5:c.785T>G	ENSP00000315602.5:p.Val262Gly
ENST00000348639.7:c.785T>G	ENSP00000267951.4:p.Val262Gly
ENST00000558903.1:n.492T>G
ENST00000559658.5:c.785T>G	ENSP00000452896.1:p.Val262Gly
NM_000743.4:c.785T>G	NP_000734.2:p.Val262Gly
NM_001166694.1:c.785T>G	NP_001160166.1:p.Val262Gly
NR_046313.1:n.1286T>G
XM_006720382.1:c.584T>G	XP_006720445.1:p.Val195Gly
XM_011521173.1:c.704T>G	XP_011519475.1:p.Val235Gly
XM_006720382.3:c.584T>G	XP_006720445.1:p.Val195Gly
NM_000743.5:c.785T>G MANE Select	NP_000734.2:p.Val262Gly
NM_001166694.2:c.785T>G	NP_001160166.1:p.Val262Gly
NR_046313.2:n.987T>G