Canonical Allele Identifier: CA342631049

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154544191G>C (hg19) ; chr1:g.154571715G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571715G>C , CM000663.2:g.154571715G>C	GRCh38
NC_000001.10:g.154544191G>C , CM000663.1:g.154544191G>C	GRCh37
NC_000001.9:g.152810815G>C	NCBI36
NG_008027.1:g.8935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.892G>C MANE Select	ENSP00000357461.3:p.Gly298Arg
ENST00000636034.1:c.892G>C	ENSP00000489703.1:p.Gly298Arg
ENST00000637900.1:c.898G>C	ENSP00000490474.1:p.Gly300Arg
ENST00000368476.3:c.892G>C	ENSP00000357461.3:p.Gly298Arg
NM_000748.2:c.892G>C	NP_000739.1:p.Gly298Arg
XM_017000180.2:c.382G>C	XP_016855669.1:p.Gly128Arg
XR_001736952.2:n.1144G>C
NM_000748.3:c.892G>C MANE Select	NP_000739.1:p.Gly298Arg