Canonical Allele Identifier: CA2189599087

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053101024

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595968C>T , CM000677.2:g.78595968C>T	GRCh38
NC_000015.9:g.78888310C>T , CM000677.1:g.78888310C>T	GRCh37
NC_000015.8:g.76675365C>T	NCBI36
NG_016143.1:g.30328G>A
NG_023328.1:g.35449C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*636G>A MANE Select	ENSP00000315602.5:n.*636G>A
ENST00000326828.5:c.*636G>A	ENSP00000315602.5:n.*636G>A
ENST00000348639.7:c.1390-2777G>A	ENSP00000267951.4:n.1390-2777G>A
ENST00000559002.5:n.193+572G>A
ENST00000559658.5:c.*64+572G>A	ENSP00000452896.1:n.*64+572G>A
NM_000743.4:c.*636G>A	NP_000734.2:n.*636G>A
NM_001166694.1:c.1390-2777G>A	NP_001160166.1:n.1390-2777G>A
NR_046313.1:n.2083+572G>A
XM_006720382.1:c.*636G>A	XP_006720445.1:n.*636G>A
XM_011521173.1:c.*636G>A	XP_011519475.1:n.*636G>A
XM_006720382.3:c.*636G>A	XP_006720445.1:n.*636G>A
NM_000743.5:c.*636G>A MANE Select	NP_000734.2:n.*636G>A
NM_001166694.2:c.1390-2777G>A	NP_001160166.1:n.1390-2777G>A
NR_046313.2:n.1784+572G>A