Canonical Allele Identifier: CA30837733

Gene: CHRNB2

Linked Data

• dbSNP Id: rs927150974
• gnomAD v3: 1-154576116-G-A
• gnomAD v4: 1-154576116-G-A
• MyVariant Identifiers: chr1:g.154576116G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154576116G>A , CM000663.2:g.154576116G>A	GRCh38
NC_000001.10:g.154548592G>A , CM000663.1:g.154548592G>A	GRCh37
NC_000001.9:g.152815216G>A	NCBI36
NG_008027.1:g.13336G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.*184G>A MANE Select	ENSP00000357461.3:n.*184G>A
ENST00000636034.1:c.1505+188G>A	ENSP00000489703.1:n.1505+188G>A
ENST00000637900.1:c.*184G>A	ENSP00000490474.1:n.*184G>A
ENST00000368476.3:c.*184G>A	ENSP00000357461.3:n.*184G>A
NM_000748.2:c.*184G>A	NP_000739.1:n.*184G>A
XM_017000180.2:c.*184G>A	XP_016855669.1:n.*184G>A
XR_001736952.2:n.1945G>A
NM_000748.3:c.*184G>A MANE Select	NP_000739.1:n.*184G>A