Canonical Allele Identifier: CA526407522

Gene: CHRNB2

Linked Data

• dbSNP Id: rs1451247550
• gnomAD v2: 1-154543646-T-A
• gnomAD v4: 1-154571170-T-A
• MyVariant Identifiers: chr1:g.154543646T>A (hg19) ; chr1:g.154571170T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571170T>A , CM000663.2:g.154571170T>A	GRCh38
NC_000001.10:g.154543646T>A , CM000663.1:g.154543646T>A	GRCh37
NC_000001.9:g.152810270T>A	NCBI36
NG_008027.1:g.8390T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.366-19T>A MANE Select	ENSP00000357461.3:n.366-19T>A
ENST00000636034.1:c.366-19T>A	ENSP00000489703.1:n.366-19T>A
ENST00000637900.1:c.372-19T>A	ENSP00000490474.1:n.372-19T>A
ENST00000368476.3:c.366-19T>A	ENSP00000357461.3:n.366-19T>A
NM_000748.2:c.366-19T>A	NP_000739.1:n.366-19T>A
XM_017000180.2:c.-9-155T>A	XP_016855669.1:n.-9-155T>A
XR_001736952.2:n.618-19T>A
NM_000748.3:c.366-19T>A MANE Select	NP_000739.1:n.366-19T>A