Canonical Allele Identifier: CA342630437

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154543895C>G (hg19) ; chr1:g.154571419C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571419C>G , CM000663.2:g.154571419C>G	GRCh38
NC_000001.10:g.154543895C>G , CM000663.1:g.154543895C>G	GRCh37
NC_000001.9:g.152810519C>G	NCBI36
NG_008027.1:g.8639C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.596C>G MANE Select	ENSP00000357461.3:p.Pro199Arg
ENST00000636034.1:c.596C>G	ENSP00000489703.1:p.Pro199Arg
ENST00000637900.1:c.602C>G	ENSP00000490474.1:p.Pro201Arg
ENST00000368476.3:c.596C>G	ENSP00000357461.3:p.Pro199Arg
NM_000748.2:c.596C>G	NP_000739.1:p.Pro199Arg
XM_017000180.2:c.86C>G	XP_016855669.1:p.Pro29Arg
XR_001736952.2:n.848C>G
NM_000748.3:c.596C>G MANE Select	NP_000739.1:p.Pro199Arg