Canonical Allele Identifier: CA421231358

Gene: CHRNB2

Linked Data

• dbSNP Id: rs1278331586
• MyVariant Identifiers: chr1:g.154544226C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571750C>T , CM000663.2:g.154571750C>T	GRCh38
NC_000001.10:g.154544226C>T , CM000663.1:g.154544226C>T	GRCh37
NC_000001.9:g.152810850C>T	NCBI36
NG_008027.1:g.8970C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.927C>T MANE Select	ENSP00000357461.3:p.Thr309=
ENST00000636034.1:c.927C>T	ENSP00000489703.1:p.Thr309=
ENST00000637900.1:c.933C>T	ENSP00000490474.1:p.Thr311=
ENST00000368476.3:c.927C>T	ENSP00000357461.3:p.Thr309=
NM_000748.2:c.927C>T	NP_000739.1:p.Thr309=
XM_017000180.2:c.417C>T	XP_016855669.1:p.Thr139=
XR_001736952.2:n.1179C>T
NM_000748.3:c.927C>T MANE Select	NP_000739.1:p.Thr309=