Canonical Allele Identifier: CA2648173031

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154576075-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154576080del , CM000663.2:g.154576080del	GRCh38
NC_000001.10:g.154548556del , CM000663.1:g.154548556del	GRCh37
NC_000001.9:g.152815180del	NCBI36
NG_008027.1:g.13300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.*148del MANE Select	ENSP00000357461.3:n.*148del
ENST00000636034.1:c.1505+152del	ENSP00000489703.1:n.1505+152del
ENST00000637900.1:c.*148del	ENSP00000490474.1:n.*148del
ENST00000368476.3:c.*148del	ENSP00000357461.3:n.*148del
NM_000748.2:c.*148del	NP_000739.1:n.*148del
XM_017000180.2:c.*148del	XP_016855669.1:n.*148del
XR_001736952.2:n.1909del
NM_000748.3:c.*148del MANE Select	NP_000739.1:n.*148del