Canonical Allele Identifier: CA342631100

Gene: CHRNB2

Linked Data

• COSMIC: COSM675850
• MyVariant Identifiers: chr1:g.154544213T>C (hg19) ; chr1:g.154571737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571737T>C , CM000663.2:g.154571737T>C	GRCh38
NC_000001.10:g.154544213T>C , CM000663.1:g.154544213T>C	GRCh37
NC_000001.9:g.152810837T>C	NCBI36
NG_008027.1:g.8957T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.914T>C MANE Select	ENSP00000357461.3:p.Met305Thr
ENST00000636034.1:c.914T>C	ENSP00000489703.1:p.Met305Thr
ENST00000637900.1:c.920T>C	ENSP00000490474.1:p.Met307Thr
ENST00000368476.3:c.914T>C	ENSP00000357461.3:p.Met305Thr
NM_000748.2:c.914T>C	NP_000739.1:p.Met305Thr
XM_017000180.2:c.404T>C	XP_016855669.1:p.Met135Thr
XR_001736952.2:n.1166T>C
NM_000748.3:c.914T>C MANE Select	NP_000739.1:p.Met305Thr