Canonical Allele Identifier: CA2648170611

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154571687-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571687_154571688insA , CM000663.2:g.154571687_154571688insA	GRCh38
NC_000001.10:g.154544163_154544164insA , CM000663.1:g.154544163_154544164insA	GRCh37
NC_000001.9:g.152810787_152810788insA	NCBI36
NG_008027.1:g.8907_8908insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.864_865insA MANE Select	ENSP00000357461.3:p.Pro289ThrfsTer?
ENST00000636034.1:c.864_865insA	ENSP00000489703.1:p.Pro289ThrfsTer?
ENST00000637900.1:c.870_871insA	ENSP00000490474.1:p.Pro291ThrfsTer?
ENST00000368476.3:c.864_865insA	ENSP00000357461.3:p.Pro289ThrfsTer?
NM_000748.2:c.864_865insA	NP_000739.1:p.Pro289ThrfsTer?
XM_017000180.2:c.354_355insA	XP_016855669.1:p.Pro119ThrfsTer?
XR_001736952.2:n.1116_1117insA
NM_000748.3:c.864_865insA MANE Select	NP_000739.1:p.Pro289ThrfsTer?