Canonical Allele Identifier: CA421230965

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154544016C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571540C>T , CM000663.2:g.154571540C>T	GRCh38
NC_000001.10:g.154544016C>T , CM000663.1:g.154544016C>T	GRCh37
NC_000001.9:g.152810640C>T	NCBI36
NG_008027.1:g.8760C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.717C>T MANE Select	ENSP00000357461.3:p.Ile239=
ENST00000636034.1:c.717C>T	ENSP00000489703.1:p.Ile239=
ENST00000637900.1:c.723C>T	ENSP00000490474.1:p.Ile241=
ENST00000368476.3:c.717C>T	ENSP00000357461.3:p.Ile239=
NM_000748.2:c.717C>T	NP_000739.1:p.Ile239=
XM_017000180.2:c.207C>T	XP_016855669.1:p.Ile69=
XR_001736952.2:n.969C>T
NM_000748.3:c.717C>T MANE Select	NP_000739.1:p.Ile239=