Canonical Allele Identifier: CA273900334

Gene: CHRNA3

Linked Data

• dbSNP Id: rs79150488
• MyVariant Identifiers: chr15:g.78888339C>T (hg19) ; chr15:g.78595997C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595997C>T , CM000677.2:g.78595997C>T	GRCh38
NC_000015.9:g.78888339C>T , CM000677.1:g.78888339C>T	GRCh37
NC_000015.8:g.76675394C>T	NCBI36
NG_016143.1:g.30299G>A
NG_023328.1:g.35478C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*607G>A MANE Select	ENSP00000315602.5:n.*607G>A
ENST00000326828.5:c.*607G>A	ENSP00000315602.5:n.*607G>A
ENST00000348639.7:c.1390-2806G>A	ENSP00000267951.4:n.1390-2806G>A
ENST00000559002.5:n.193+543G>A
ENST00000559658.5:c.*64+543G>A	ENSP00000452896.1:n.*64+543G>A
NM_000743.4:c.*607G>A	NP_000734.2:n.*607G>A
NM_001166694.1:c.1390-2806G>A	NP_001160166.1:n.1390-2806G>A
NR_046313.1:n.2083+543G>A
XM_006720382.1:c.*607G>A	XP_006720445.1:n.*607G>A
XM_011521173.1:c.*607G>A	XP_011519475.1:n.*607G>A
XM_006720382.3:c.*607G>A	XP_006720445.1:n.*607G>A
NM_000743.5:c.*607G>A MANE Select	NP_000734.2:n.*607G>A
NM_001166694.2:c.1390-2806G>A	NP_001160166.1:n.1390-2806G>A
NR_046313.2:n.1784+543G>A