Canonical Allele Identifier: CA342631120

Gene: CHRNB2

Linked Data

• dbSNP Id: rs777476359
• MyVariant Identifiers: chr1:g.154544224A>C (hg19) ; chr1:g.154571748A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571748A>C , CM000663.2:g.154571748A>C	GRCh38
NC_000001.10:g.154544224A>C , CM000663.1:g.154544224A>C	GRCh37
NC_000001.9:g.152810848A>C	NCBI36
NG_008027.1:g.8968A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.925A>C MANE Select	ENSP00000357461.3:p.Thr309Pro
ENST00000636034.1:c.925A>C	ENSP00000489703.1:p.Thr309Pro
ENST00000637900.1:c.931A>C	ENSP00000490474.1:p.Thr311Pro
ENST00000368476.3:c.925A>C	ENSP00000357461.3:p.Thr309Pro
NM_000748.2:c.925A>C	NP_000739.1:p.Thr309Pro
XM_017000180.2:c.415A>C	XP_016855669.1:p.Thr139Pro
XR_001736952.2:n.1177A>C
NM_000748.3:c.925A>C MANE Select	NP_000739.1:p.Thr309Pro