Canonical Allele Identifier: CA421231357

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154544226C>G (hg19)

Genomic Alleles

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

Transcript Alleles

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