Canonical Allele Identifier: CA273900311

Gene: CHRNA3

Linked Data

• dbSNP Id: rs199846852
• gnomAD v3: 15-78595987-T-C
• gnomAD v4: 15-78595987-T-C
• MyVariant Identifiers: chr15:g.78888329T>C (hg19) ; chr15:g.78595987T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595987T>C , CM000677.2:g.78595987T>C	GRCh38
NC_000015.9:g.78888329T>C , CM000677.1:g.78888329T>C	GRCh37
NC_000015.8:g.76675384T>C	NCBI36
NG_016143.1:g.30309A>G
NG_023328.1:g.35468T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*617A>G MANE Select	ENSP00000315602.5:n.*617A>G
ENST00000326828.5:c.*617A>G	ENSP00000315602.5:n.*617A>G
ENST00000348639.7:c.1390-2796A>G	ENSP00000267951.4:n.1390-2796A>G
ENST00000559002.5:n.193+553A>G
ENST00000559658.5:c.*64+553A>G	ENSP00000452896.1:n.*64+553A>G
NM_000743.4:c.*617A>G	NP_000734.2:n.*617A>G
NM_001166694.1:c.1390-2796A>G	NP_001160166.1:n.1390-2796A>G
NR_046313.1:n.2083+553A>G
XM_006720382.1:c.*617A>G	XP_006720445.1:n.*617A>G
XM_011521173.1:c.*617A>G	XP_011519475.1:n.*617A>G
XM_006720382.3:c.*617A>G	XP_006720445.1:n.*617A>G
NM_000743.5:c.*617A>G MANE Select	NP_000734.2:n.*617A>G
NM_001166694.2:c.1390-2796A>G	NP_001160166.1:n.1390-2796A>G
NR_046313.2:n.1784+553A>G