Canonical Allele Identifier: CA889597617

Gene: CHRNB2

Linked Data

• dbSNP Id: rs1326255609
• gnomAD v3: 1-154569376-G-A
• gnomAD v4: 1-154569376-G-A
• MyVariant Identifiers: chr1:g.154541852G>A (hg19) ; chr1:g.154569376G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154569376G>A , CM000663.2:g.154569376G>A	GRCh38
NC_000001.10:g.154541852G>A , CM000663.1:g.154541852G>A	GRCh37
NC_000001.9:g.152808476G>A	NCBI36
NG_008027.1:g.6596G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368476.4:c.65-86G>A MANE Select	ENSP00000357461.3:n.65-86G>A
ENST00000636034.1:c.65-86G>A	ENSP00000489703.1:n.65-86G>A
ENST00000637900.1:c.65-86G>A	ENSP00000490474.1:n.65-86G>A
ENST00000368476.3:c.65-86G>A	ENSP00000357461.3:n.65-86G>A
NM_000748.2:c.65-86G>A	NP_000739.1:n.65-86G>A
XM_017000180.2:c.-310-86G>A	XP_016855669.1:n.-310-86G>A
XR_001736952.2:n.317-86G>A
NM_000748.3:c.65-86G>A MANE Select	NP_000739.1:n.65-86G>A