Canonical Allele Identifier: CA2733119326

Gene: CHRNB1

Linked Data

• dbSNP Id: rs2150842241

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454079_7454080del , CM000679.2:g.7454079_7454080del	GRCh38
NC_000017.10:g.7357398_7357399del , CM000679.1:g.7357398_7357399del	GRCh37
NC_000017.9:g.7298122_7298123del	NCBI36
NG_008026.1:g.13993_13994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.821-218_821-217del MANE Select	ENSP00000304290.2:n.821-218_821-217del
ENST00000306071.6:c.821-218_821-217del	ENSP00000304290.2:n.821-218_821-217del
ENST00000536404.6:c.605-218_605-217del	ENSP00000439209.2:n.605-218_605-217del
ENST00000570557.5:c.484-218_484-217del
ENST00000573209.1:n.1765-218_1765-217del
ENST00000576360.1:c.605-365_605-364del	ENSP00000459092.1:n.605-365_605-364del
NM_000747.2:c.821-218_821-217del	NP_000738.2:n.821-218_821-217del
NM_000747.3:c.821-218_821-217del MANE Select	NP_000738.2:n.821-218_821-217del