Canonical Allele Identifier: CA421231255

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154544172C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571696C>T , CM000663.2:g.154571696C>T	GRCh38
NC_000001.10:g.154544172C>T , CM000663.1:g.154544172C>T	GRCh37
NC_000001.9:g.152810796C>T	NCBI36
NG_008027.1:g.8916C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.873C>T MANE Select	ENSP00000357461.3:p.Ser291=
ENST00000636034.1:c.873C>T	ENSP00000489703.1:p.Ser291=
ENST00000637900.1:c.879C>T	ENSP00000490474.1:p.Ser293=
ENST00000368476.3:c.873C>T	ENSP00000357461.3:p.Ser291=
NM_000748.2:c.873C>T	NP_000739.1:p.Ser291=
XM_017000180.2:c.363C>T	XP_016855669.1:p.Ser121=
XR_001736952.2:n.1125C>T
NM_000748.3:c.873C>T MANE Select	NP_000739.1:p.Ser291=