Canonical Allele Identifier: CA421231327

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154544217G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571741G>T , CM000663.2:g.154571741G>T	GRCh38
NC_000001.10:g.154544217G>T , CM000663.1:g.154544217G>T	GRCh37
NC_000001.9:g.152810841G>T	NCBI36
NG_008027.1:g.8961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.918G>T MANE Select	ENSP00000357461.3:p.Val306=
ENST00000636034.1:c.918G>T	ENSP00000489703.1:p.Val306=
ENST00000637900.1:c.924G>T	ENSP00000490474.1:p.Val308=
ENST00000368476.3:c.918G>T	ENSP00000357461.3:p.Val306=
NM_000748.2:c.918G>T	NP_000739.1:p.Val306=
XM_017000180.2:c.408G>T	XP_016855669.1:p.Val136=
XR_001736952.2:n.1170G>T
NM_000748.3:c.918G>T MANE Select	NP_000739.1:p.Val306=