Canonical Allele Identifier: CA273903199

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1049408758
• MyVariant Identifiers: chr15:g.78599185C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78599185C>G , CM000677.2:g.78599185C>G	GRCh38
NC_000015.9:g.78891527C>G , CM000677.1:g.78891527C>G	GRCh37
NC_000015.8:g.76678582C>G	NCBI36
NG_016143.1:g.27111G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.1389+2068G>C MANE Select	ENSP00000315602.5:n.1389+2068G>C
ENST00000326828.5:c.1389+2068G>C	ENSP00000315602.5:n.1389+2068G>C
ENST00000348639.7:c.1389+2068G>C	ENSP00000267951.4:n.1389+2068G>C
ENST00000559658.5:c.1389+2068G>C	ENSP00000452896.1:n.1389+2068G>C
NM_000743.4:c.1389+2068G>C	NP_000734.2:n.1389+2068G>C
NM_001166694.1:c.1389+2068G>C	NP_001160166.1:n.1389+2068G>C
NR_046313.1:n.1890+2068G>C
XM_006720382.1:c.1188+2068G>C	XP_006720445.1:n.1188+2068G>C
XM_011521173.1:c.1308+2068G>C	XP_011519475.1:n.1308+2068G>C
XM_006720382.3:c.1188+2068G>C	XP_006720445.1:n.1188+2068G>C
NM_000743.5:c.1389+2068G>C MANE Select	NP_000734.2:n.1389+2068G>C
NM_001166694.2:c.1389+2068G>C	NP_001160166.1:n.1389+2068G>C
NR_046313.2:n.1591+2068G>C