Canonical Allele Identifier: CA273896108

Gene: CHRNA5

Linked Data

• dbSNP Id: rs1018181118
• MyVariant Identifiers: chr15:g.78882937T>C (hg19) ; chr15:g.78590595T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78590595T>C , CM000677.2:g.78590595T>C	GRCh38
NC_000015.9:g.78882937T>C , CM000677.1:g.78882937T>C	GRCh37
NC_000015.8:g.76669992T>C	NCBI36
NG_023328.1:g.30076T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299565.9:c.1204T>C MANE Select	ENSP00000299565.5:p.Tyr402His
ENST00000394802.4:c.522+497T>C
ENST00000559554.5:c.458+746T>C	ENSP00000453519.1:n.458+746T>C
ENST00000559576.1:c.145+89T>C
NM_000745.3:c.1204T>C	NP_000736.2:p.Tyr402His
NM_001307945.1:c.458+746T>C	NP_001294874.1:n.458+746T>C
XM_005254142.2:c.707+497T>C	XP_005254199.1:n.707+497T>C
NM_001307945.2:c.458+746T>C	NP_001294874.1:n.458+746T>C
NM_000745.4:c.1204T>C MANE Select	NP_000736.2:p.Tyr402His
NM_001395171.1:c.1115+89T>C	NP_001382100.1:n.1115+89T>C
NM_001395172.1:c.591+613T>C	NP_001382101.1:n.591+613T>C
NM_001395173.1:c.713+491T>C	NP_001382102.1:n.713+491T>C
NM_001395174.1:c.707+497T>C	NP_001382103.1:n.707+497T>C
NM_001395175.1:c.455+746T>C	NP_001382104.1:n.455+746T>C