Canonical Allele Identifier: CA421230933

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154543836C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571360C>T , CM000663.2:g.154571360C>T	GRCh38
NC_000001.10:g.154543836C>T , CM000663.1:g.154543836C>T	GRCh37
NC_000001.9:g.152810460C>T	NCBI36
NG_008027.1:g.8580C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.537C>T MANE Select	ENSP00000357461.3:p.Asp179=
ENST00000636034.1:c.537C>T	ENSP00000489703.1:p.Asp179=
ENST00000637900.1:c.543C>T	ENSP00000490474.1:p.Asp181=
ENST00000368476.3:c.537C>T	ENSP00000357461.3:p.Asp179=
NM_000748.2:c.537C>T	NP_000739.1:p.Asp179=
XM_017000180.2:c.27C>T	XP_016855669.1:p.Asp9=
XR_001736952.2:n.789C>T
NM_000748.3:c.537C>T MANE Select	NP_000739.1:p.Asp179=