Canonical Allele Identifier: CA2189585591

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1567073275

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78599314T>C , CM000677.2:g.78599314T>C	GRCh38
NC_000015.9:g.78891656T>C , CM000677.1:g.78891656T>C	GRCh37
NC_000015.8:g.76678711T>C	NCBI36
NG_016143.1:g.26982A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.1389+1939A>G MANE Select	ENSP00000315602.5:n.1389+1939A>G
ENST00000326828.5:c.1389+1939A>G	ENSP00000315602.5:n.1389+1939A>G
ENST00000348639.7:c.1389+1939A>G	ENSP00000267951.4:n.1389+1939A>G
ENST00000559658.5:c.1389+1939A>G	ENSP00000452896.1:n.1389+1939A>G
NM_000743.4:c.1389+1939A>G	NP_000734.2:n.1389+1939A>G
NM_001166694.1:c.1389+1939A>G	NP_001160166.1:n.1389+1939A>G
NR_046313.1:n.1890+1939A>G
XM_006720382.1:c.1188+1939A>G	XP_006720445.1:n.1188+1939A>G
XM_011521173.1:c.1308+1939A>G	XP_011519475.1:n.1308+1939A>G
XM_006720382.3:c.1188+1939A>G	XP_006720445.1:n.1188+1939A>G
NM_000743.5:c.1389+1939A>G MANE Select	NP_000734.2:n.1389+1939A>G
NM_001166694.2:c.1389+1939A>G	NP_001160166.1:n.1389+1939A>G
NR_046313.2:n.1591+1939A>G