Canonical Allele Identifier: CA273900411

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1014488469
• gnomAD v4: 15-78596070-A-G
• MyVariant Identifiers: chr15:g.78888412A>G (hg19) ; chr15:g.78596070A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78596070A>G , CM000677.2:g.78596070A>G	GRCh38
NC_000015.9:g.78888412A>G , CM000677.1:g.78888412A>G	GRCh37
NC_000015.8:g.76675467A>G	NCBI36
NG_016143.1:g.30226T>C
NG_023328.1:g.35551A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*534T>C MANE Select	ENSP00000315602.5:n.*534T>C
ENST00000326828.5:c.*534T>C	ENSP00000315602.5:n.*534T>C
ENST00000348639.7:c.1390-2879T>C	ENSP00000267951.4:n.1390-2879T>C
ENST00000559002.5:n.193+470T>C
ENST00000559658.5:c.*64+470T>C	ENSP00000452896.1:n.*64+470T>C
NM_000743.4:c.*534T>C	NP_000734.2:n.*534T>C
NM_001166694.1:c.1390-2879T>C	NP_001160166.1:n.1390-2879T>C
NR_046313.1:n.2083+470T>C
XM_006720382.1:c.*534T>C	XP_006720445.1:n.*534T>C
XM_011521173.1:c.*534T>C	XP_011519475.1:n.*534T>C
XM_006720382.3:c.*534T>C	XP_006720445.1:n.*534T>C
NM_000743.5:c.*534T>C MANE Select	NP_000734.2:n.*534T>C
NM_001166694.2:c.1390-2879T>C	NP_001160166.1:n.1390-2879T>C
NR_046313.2:n.1784+470T>C