Canonical Allele Identifier: CA15852490
Gene: CHRNA5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17408276

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78589276T>C , CM000677.2:g.78589276T>C GRCh38
NC_000015.9:g.78881618T>C , CM000677.1:g.78881618T>C GRCh37
NC_000015.8:g.76668673T>C NCBI36
NG_023328.1:g.28757T>C

Transcript Alleles

HGVS Amino-acid change
NM_000745.3:c.414-529T>C VV NP_000736.2:p.=
NM_001307945.1:c.414-529T>C VV NP_001294874.1:p.=
XM_005254142.2:c.414-529T>C XP_005254199.1:p.=
ENST00000299565.9:c.414-529T>C ENSP00000299565.5:p.=
ENST00000394802.4:n.229-529T>C
ENST00000559554.5:c.414-529T>C ENSP00000453519.1:p.=