Canonical Allele Identifier: CA421231005

Gene: CHRNB2

Linked Data

• COSMIC: COSM6058383
• MyVariant Identifiers: chr1:g.154544067C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571591C>T , CM000663.2:g.154571591C>T	GRCh38
NC_000001.10:g.154544067C>T , CM000663.1:g.154544067C>T	GRCh37
NC_000001.9:g.152810691C>T	NCBI36
NG_008027.1:g.8811C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.768C>T MANE Select	ENSP00000357461.3:p.Phe256=
ENST00000636034.1:c.768C>T	ENSP00000489703.1:p.Phe256=
ENST00000637900.1:c.774C>T	ENSP00000490474.1:p.Phe258=
ENST00000368476.3:c.768C>T	ENSP00000357461.3:p.Phe256=
NM_000748.2:c.768C>T	NP_000739.1:p.Phe256=
XM_017000180.2:c.258C>T	XP_016855669.1:p.Phe86=
XR_001736952.2:n.1020C>T
NM_000748.3:c.768C>T MANE Select	NP_000739.1:p.Phe256=