Canonical Allele Identifier: CA421231365

Gene: CHRNB2

Linked Data

• COSMIC: COSM1334454
• MyVariant Identifiers: chr1:g.154543996_154543997insA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571521dup , CM000663.2:g.154571521dup	GRCh38
NC_000001.10:g.154543997dup , CM000663.1:g.154543997dup	GRCh37
NC_000001.9:g.152810621dup	NCBI36
NG_008027.1:g.8741dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.698dup MANE Select	ENSP00000357461.3:p.Pro234AlafsTer?
ENST00000636034.1:c.698dup	ENSP00000489703.1:p.Pro234AlafsTer?
ENST00000637900.1:c.704dup	ENSP00000490474.1:p.Pro236AlafsTer?
ENST00000368476.3:c.698dup	ENSP00000357461.3:p.Pro234AlafsTer?
NM_000748.2:c.698dup	NP_000739.1:p.Pro234AlafsTer?
XM_017000180.2:c.188dup	XP_016855669.1:p.Pro64AlafsTer?
XR_001736952.2:n.950dup
NM_000748.3:c.698dup MANE Select	NP_000739.1:p.Pro234AlafsTer?