Canonical Allele Identifier: CA2648171635

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154569375-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154569377del , CM000663.2:g.154569377del	GRCh38
NC_000001.10:g.154541853del , CM000663.1:g.154541853del	GRCh37
NC_000001.9:g.152808477del	NCBI36
NG_008027.1:g.6597del

Transcript Alleles

HGVS	Amino-acid change
ENST00000368476.4:c.65-85del MANE Select	ENSP00000357461.3:n.65-85del
ENST00000636034.1:c.65-85del	ENSP00000489703.1:n.65-85del
ENST00000637900.1:c.65-85del	ENSP00000490474.1:n.65-85del
ENST00000368476.3:c.65-85del	ENSP00000357461.3:n.65-85del
NM_000748.2:c.65-85del	NP_000739.1:n.65-85del
XM_017000180.2:c.-310-85del	XP_016855669.1:n.-310-85del
XR_001736952.2:n.317-85del
NM_000748.3:c.65-85del MANE Select	NP_000739.1:n.65-85del