Canonical Allele Identifier: CA2189585594

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053160836

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78599315T>G , CM000677.2:g.78599315T>G	GRCh38
NC_000015.9:g.78891657T>G , CM000677.1:g.78891657T>G	GRCh37
NC_000015.8:g.76678712T>G	NCBI36
NG_016143.1:g.26981A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.1389+1938A>C MANE Select	ENSP00000315602.5:n.1389+1938A>C
ENST00000326828.5:c.1389+1938A>C	ENSP00000315602.5:n.1389+1938A>C
ENST00000348639.7:c.1389+1938A>C	ENSP00000267951.4:n.1389+1938A>C
ENST00000559658.5:c.1389+1938A>C	ENSP00000452896.1:n.1389+1938A>C
NM_000743.4:c.1389+1938A>C	NP_000734.2:n.1389+1938A>C
NM_001166694.1:c.1389+1938A>C	NP_001160166.1:n.1389+1938A>C
NR_046313.1:n.1890+1938A>C
XM_006720382.1:c.1188+1938A>C	XP_006720445.1:n.1188+1938A>C
XM_011521173.1:c.1308+1938A>C	XP_011519475.1:n.1308+1938A>C
XM_006720382.3:c.1188+1938A>C	XP_006720445.1:n.1188+1938A>C
NM_000743.5:c.1389+1938A>C MANE Select	NP_000734.2:n.1389+1938A>C
NM_001166694.2:c.1389+1938A>C	NP_001160166.1:n.1389+1938A>C
NR_046313.2:n.1591+1938A>C