Canonical Allele Identifier: CA421231101

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154544112A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571636A>T , CM000663.2:g.154571636A>T	GRCh38
NC_000001.10:g.154544112A>T , CM000663.1:g.154544112A>T	GRCh37
NC_000001.9:g.152810736A>T	NCBI36
NG_008027.1:g.8856A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.813A>T MANE Select	ENSP00000357461.3:p.Ser271=
ENST00000636034.1:c.813A>T	ENSP00000489703.1:p.Ser271=
ENST00000637900.1:c.819A>T	ENSP00000490474.1:p.Ser273=
ENST00000368476.3:c.813A>T	ENSP00000357461.3:p.Ser271=
NM_000748.2:c.813A>T	NP_000739.1:p.Ser271=
XM_017000180.2:c.303A>T	XP_016855669.1:p.Ser101=
XR_001736952.2:n.1065A>T
NM_000748.3:c.813A>T MANE Select	NP_000739.1:p.Ser271=