Canonical Allele Identifier: CA715973455

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1208029234
• gnomAD v3: 15-78615599-C-A
• gnomAD v4: 15-78615599-C-A
• MyVariant Identifiers: chr15:g.78907941C>A (hg19) ; chr15:g.78615599C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615599C>A , CM000677.2:g.78615599C>A	GRCh38
NC_000015.9:g.78907941C>A , CM000677.1:g.78907941C>A	GRCh37
NC_000015.8:g.76694996C>A	NCBI36
NG_016143.1:g.10697G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1425G>T MANE Select	ENSP00000315602.5:n.377+1425G>T
ENST00000326828.5:c.377+1425G>T	ENSP00000315602.5:n.377+1425G>T
ENST00000348639.7:c.377+1425G>T	ENSP00000267951.4:n.377+1425G>T
ENST00000559658.5:c.377+1425G>T	ENSP00000452896.1:n.377+1425G>T
NM_000743.4:c.377+1425G>T	NP_000734.2:n.377+1425G>T
NM_001166694.1:c.377+1425G>T	NP_001160166.1:n.377+1425G>T
NR_046313.1:n.878+1425G>T
XM_006720382.1:c.176+1425G>T	XP_006720445.1:n.176+1425G>T
XM_011521173.1:c.296+1425G>T	XP_011519475.1:n.296+1425G>T
XM_006720382.3:c.176+1425G>T	XP_006720445.1:n.176+1425G>T
NM_000743.5:c.377+1425G>T MANE Select	NP_000734.2:n.377+1425G>T
NM_001166694.2:c.377+1425G>T	NP_001160166.1:n.377+1425G>T
NR_046313.2:n.579+1425G>T