Canonical Allele Identifier: CA16510576

Gene: CHRNA3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78603787A>G , CM000677.2:g.78603787A>G	GRCh38
NC_000015.9:g.78896129A>G , CM000677.1:g.78896129A>G	GRCh37
NC_000015.8:g.76683184A>G	NCBI36
NG_016143.1:g.22509T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-1523T>C MANE Select	ENSP00000315602.5:n.378-1523T>C
ENST00000326828.5:c.378-1523T>C	ENSP00000315602.5:n.378-1523T>C
ENST00000348639.7:c.378-1523T>C	ENSP00000267951.4:n.378-1523T>C
ENST00000558903.1:n.85-1523T>C
ENST00000559658.5:c.378-1523T>C	ENSP00000452896.1:n.378-1523T>C
NM_000743.4:c.378-1523T>C	NP_000734.2:n.378-1523T>C
NM_001166694.1:c.378-1523T>C	NP_001160166.1:n.378-1523T>C
NR_046313.1:n.879-1523T>C
XM_006720382.1:c.177-1523T>C	XP_006720445.1:n.177-1523T>C
XM_011521173.1:c.297-1523T>C	XP_011519475.1:n.297-1523T>C
XM_006720382.3:c.177-1523T>C	XP_006720445.1:n.177-1523T>C
NM_000743.5:c.378-1523T>C MANE Select	NP_000734.2:n.378-1523T>C
NM_001166694.2:c.378-1523T>C	NP_001160166.1:n.378-1523T>C
NR_046313.2:n.580-1523T>C