Canonical Allele Identifier: CA421231157

Gene: CHRNB2

Linked Data

• dbSNP Id: rs1190451612
• gnomAD v3: 1-154571654-G-T
• gnomAD v4: 1-154571654-G-T
• MyVariant Identifiers: chr1:g.154544130G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571654G>T , CM000663.2:g.154571654G>T	GRCh38
NC_000001.10:g.154544130G>T , CM000663.1:g.154544130G>T	GRCh37
NC_000001.9:g.152810754G>T	NCBI36
NG_008027.1:g.8874G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.831G>T MANE Select	ENSP00000357461.3:p.Thr277=
ENST00000636034.1:c.831G>T	ENSP00000489703.1:p.Thr277=
ENST00000637900.1:c.837G>T	ENSP00000490474.1:p.Thr279=
ENST00000368476.3:c.831G>T	ENSP00000357461.3:p.Thr277=
NM_000748.2:c.831G>T	NP_000739.1:p.Thr277=
XM_017000180.2:c.321G>T	XP_016855669.1:p.Thr107=
XR_001736952.2:n.1083G>T
NM_000748.3:c.831G>T MANE Select	NP_000739.1:p.Thr277=