Canonical Allele Identifier: CA342630537

Gene: CHRNB2

Linked Data

• dbSNP Id: rs200796605
• gnomAD v3: 1-154571469-C-G
• gnomAD v4: 1-154571469-C-G
• MyVariant Identifiers: chr1:g.154543945C>G (hg19) ; chr1:g.154571469C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571469C>G , CM000663.2:g.154571469C>G	GRCh38
NC_000001.10:g.154543945C>G , CM000663.1:g.154543945C>G	GRCh37
NC_000001.9:g.152810569C>G	NCBI36
NG_008027.1:g.8689C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.646C>G MANE Select	ENSP00000357461.3:p.Pro216Ala
ENST00000636034.1:c.646C>G	ENSP00000489703.1:p.Pro216Ala
ENST00000637900.1:c.652C>G	ENSP00000490474.1:p.Pro218Ala
ENST00000368476.3:c.646C>G	ENSP00000357461.3:p.Pro216Ala
NM_000748.2:c.646C>G	NP_000739.1:p.Pro216Ala
XM_017000180.2:c.136C>G	XP_016855669.1:p.Pro46Ala
XR_001736952.2:n.898C>G
NM_000748.3:c.646C>G MANE Select	NP_000739.1:p.Pro216Ala