Canonical Allele Identifier: CA342631169

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154544248T>G (hg19) ; chr1:g.154571772T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571772T>G , CM000663.2:g.154571772T>G	GRCh38
NC_000001.10:g.154544248T>G , CM000663.1:g.154544248T>G	GRCh37
NC_000001.9:g.152810872T>G	NCBI36
NG_008027.1:g.8992T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.949T>G MANE Select	ENSP00000357461.3:p.Cys317Gly
ENST00000636034.1:c.949T>G	ENSP00000489703.1:p.Cys317Gly
ENST00000637900.1:c.955T>G	ENSP00000490474.1:p.Cys319Gly
ENST00000368476.3:c.949T>G	ENSP00000357461.3:p.Cys317Gly
NM_000748.2:c.949T>G	NP_000739.1:p.Cys317Gly
XM_017000180.2:c.439T>G	XP_016855669.1:p.Cys147Gly
XR_001736952.2:n.1201T>G
NM_000748.3:c.949T>G MANE Select	NP_000739.1:p.Cys317Gly