Canonical Allele Identifier: CA526666166

Gene: CHRNB2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154572175G>A , CM000663.2:g.154572175G>A	GRCh38
NC_000001.10:g.154544651G>A , CM000663.1:g.154544651G>A	GRCh37
NC_000001.9:g.152811275G>A	NCBI36
NG_008027.1:g.9395G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.1338+14G>A MANE Select	ENSP00000357461.3:n.1338+14G>A
ENST00000636034.1:c.1338+14G>A	ENSP00000489703.1:n.1338+14G>A
ENST00000637900.1:c.1344+14G>A	ENSP00000490474.1:n.1344+14G>A
ENST00000368476.3:c.1338+14G>A	ENSP00000357461.3:n.1338+14G>A
NM_000748.2:c.1338+14G>A	NP_000739.1:n.1338+14G>A
XM_017000180.2:c.828+14G>A	XP_016855669.1:n.828+14G>A
XR_001736952.2:n.1590+14G>A
NM_000748.3:c.1338+14G>A MANE Select	NP_000739.1:n.1338+14G>A