Canonical Allele Identifier: CA273903304

Gene: CHRNA3

Linked Data

• dbSNP Id: rs766306634
• gnomAD v2: 15-78891681-A-G
• gnomAD v3: 15-78599339-A-G
• gnomAD v4: 15-78599339-A-G
• MyVariant Identifiers: chr15:g.78891681A>G (hg19) ; chr15:g.78599339A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78599339A>G , CM000677.2:g.78599339A>G	GRCh38
NC_000015.9:g.78891681A>G , CM000677.1:g.78891681A>G	GRCh37
NC_000015.8:g.76678736A>G	NCBI36
NG_016143.1:g.26957T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.1389+1914T>C MANE Select	ENSP00000315602.5:n.1389+1914T>C
ENST00000326828.5:c.1389+1914T>C	ENSP00000315602.5:n.1389+1914T>C
ENST00000348639.7:c.1389+1914T>C	ENSP00000267951.4:n.1389+1914T>C
ENST00000559658.5:c.1389+1914T>C	ENSP00000452896.1:n.1389+1914T>C
NM_000743.4:c.1389+1914T>C	NP_000734.2:n.1389+1914T>C
NM_001166694.1:c.1389+1914T>C	NP_001160166.1:n.1389+1914T>C
NR_046313.1:n.1890+1914T>C
XM_006720382.1:c.1188+1914T>C	XP_006720445.1:n.1188+1914T>C
XM_011521173.1:c.1308+1914T>C	XP_011519475.1:n.1308+1914T>C
XM_006720382.3:c.1188+1914T>C	XP_006720445.1:n.1188+1914T>C
NM_000743.5:c.1389+1914T>C MANE Select	NP_000734.2:n.1389+1914T>C
NM_001166694.2:c.1389+1914T>C	NP_001160166.1:n.1389+1914T>C
NR_046313.2:n.1591+1914T>C