Canonical Allele Identifier: CA342630848

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154544092A>T (hg19) ; chr1:g.154571616A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571616A>T , CM000663.2:g.154571616A>T	GRCh38
NC_000001.10:g.154544092A>T , CM000663.1:g.154544092A>T	GRCh37
NC_000001.9:g.152810716A>T	NCBI36
NG_008027.1:g.8836A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.793A>T MANE Select	ENSP00000357461.3:p.Lys265Ter
ENST00000636034.1:c.793A>T	ENSP00000489703.1:p.Lys265Ter
ENST00000637900.1:c.799A>T	ENSP00000490474.1:p.Lys267Ter
ENST00000368476.3:c.793A>T	ENSP00000357461.3:p.Lys265Ter
NM_000748.2:c.793A>T	NP_000739.1:p.Lys265Ter
XM_017000180.2:c.283A>T	XP_016855669.1:p.Lys95Ter
XR_001736952.2:n.1045A>T
NM_000748.3:c.793A>T MANE Select	NP_000739.1:p.Lys265Ter