Canonical Allele Identifier: CA2480925175

Gene: CHRNB2

Linked Data

• dbSNP Id: rs1696157763

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571173del , CM000663.2:g.154571173del	GRCh38
NC_000001.10:g.154543649del , CM000663.1:g.154543649del	GRCh37
NC_000001.9:g.152810273del	NCBI36
NG_008027.1:g.8393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.366-16del MANE Select	ENSP00000357461.3:n.366-16del
ENST00000636034.1:c.366-16del	ENSP00000489703.1:n.366-16del
ENST00000637900.1:c.372-16del	ENSP00000490474.1:n.372-16del
ENST00000368476.3:c.366-16del	ENSP00000357461.3:n.366-16del
NM_000748.2:c.366-16del	NP_000739.1:n.366-16del
XM_017000180.2:c.-9-152del	XP_016855669.1:n.-9-152del
XR_001736952.2:n.618-16del
NM_000748.3:c.366-16del MANE Select	NP_000739.1:n.366-16del