Canonical Allele Identifier: CA2480925262

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571469_154571470delinsCC , CM000663.2:g.154571469_154571470delinsCC	GRCh38
NC_000001.10:g.154543945_154543946delinsCC , CM000663.1:g.154543945_154543946delinsCC	GRCh37
NC_000001.9:g.152810569_152810570delinsCC	NCBI36
NG_008027.1:g.8689_8690delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.646_647delinsCC MANE Select	ENSP00000357461.3:p.Pro216=
ENST00000636034.1:c.646_647delinsCC	ENSP00000489703.1:p.Pro216=
ENST00000637900.1:c.652_653delinsCC	ENSP00000490474.1:p.Pro218=
ENST00000368476.3:c.646_647delinsCC	ENSP00000357461.3:p.Pro216=
NM_000748.2:c.646_647delinsCC	NP_000739.1:p.Pro216=
XM_017000180.2:c.136_137delinsCC	XP_016855669.1:p.Pro46=
XR_001736952.2:n.898_899delinsCC
NM_000748.3:c.646_647delinsCC MANE Select	NP_000739.1:p.Pro216=