Canonical Allele Identifier: CA2648173390

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154576220-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154576220C>T , CM000663.2:g.154576220C>T	GRCh38
NC_000001.10:g.154548696C>T , CM000663.1:g.154548696C>T	GRCh37
NC_000001.9:g.152815320C>T	NCBI36
NG_008027.1:g.13440C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.*288C>T MANE Select	ENSP00000357461.3:n.*288C>T
ENST00000636034.1:c.1505+292C>T	ENSP00000489703.1:n.1505+292C>T
ENST00000637900.1:c.*288C>T	ENSP00000490474.1:n.*288C>T
ENST00000368476.3:c.*288C>T	ENSP00000357461.3:n.*288C>T
NM_000748.2:c.*288C>T	NP_000739.1:n.*288C>T
XM_017000180.2:c.*288C>T	XP_016855669.1:n.*288C>T
XR_001736952.2:n.2049C>T
NM_000748.3:c.*288C>T MANE Select	NP_000739.1:n.*288C>T