Canonical Allele Identifier: CA342630079

Gene: CHRNB2

Linked Data

• COSMIC: COSM4928472
• MyVariant Identifiers: chr1:g.154543762T>C (hg19) ; chr1:g.154571286T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571286T>C , CM000663.2:g.154571286T>C	GRCh38
NC_000001.10:g.154543762T>C , CM000663.1:g.154543762T>C	GRCh37
NC_000001.9:g.152810386T>C	NCBI36
NG_008027.1:g.8506T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.463T>C MANE Select	ENSP00000357461.3:p.Cys155Arg
ENST00000636034.1:c.463T>C	ENSP00000489703.1:p.Cys155Arg
ENST00000637900.1:c.469T>C	ENSP00000490474.1:p.Cys157Arg
ENST00000368476.3:c.463T>C	ENSP00000357461.3:p.Cys155Arg
NM_000748.2:c.463T>C	NP_000739.1:p.Cys155Arg
XM_017000180.2:c.-9-39T>C	XP_016855669.1:n.-9-39T>C
XR_001736952.2:n.715T>C
NM_000748.3:c.463T>C MANE Select	NP_000739.1:p.Cys155Arg