Canonical Allele Identifier: CA2648170622

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154571694-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571694_154571695insA , CM000663.2:g.154571694_154571695insA	GRCh38
NC_000001.10:g.154544170_154544171insA , CM000663.1:g.154544170_154544171insA	GRCh37
NC_000001.9:g.152810794_152810795insA	NCBI36
NG_008027.1:g.8914_8915insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.871_872insA MANE Select	ENSP00000357461.3:p.Ser291TyrfsTer?
ENST00000636034.1:c.871_872insA	ENSP00000489703.1:p.Ser291TyrfsTer?
ENST00000637900.1:c.877_878insA	ENSP00000490474.1:p.Ser293TyrfsTer?
ENST00000368476.3:c.871_872insA	ENSP00000357461.3:p.Ser291TyrfsTer?
NM_000748.2:c.871_872insA	NP_000739.1:p.Ser291TyrfsTer?
XM_017000180.2:c.361_362insA	XP_016855669.1:p.Ser121TyrfsTer?
XR_001736952.2:n.1123_1124insA
NM_000748.3:c.871_872insA MANE Select	NP_000739.1:p.Ser291TyrfsTer?