Canonical Allele Identifier: CA2648170684

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154571707-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571707_154571708insAA , CM000663.2:g.154571707_154571708insAA	GRCh38
NC_000001.10:g.154544183_154544184insAA , CM000663.1:g.154544183_154544184insAA	GRCh37
NC_000001.9:g.152810807_152810808insAA	NCBI36
NG_008027.1:g.8927_8928insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.884_885insAA MANE Select	ENSP00000357461.3:p.Leu296SerfsTer?
ENST00000636034.1:c.884_885insAA	ENSP00000489703.1:p.Leu296SerfsTer?
ENST00000637900.1:c.890_891insAA	ENSP00000490474.1:p.Leu298SerfsTer?
ENST00000368476.3:c.884_885insAA	ENSP00000357461.3:p.Leu296SerfsTer?
NM_000748.2:c.884_885insAA	NP_000739.1:p.Leu296SerfsTer?
XM_017000180.2:c.374_375insAA	XP_016855669.1:p.Leu126SerfsTer?
XR_001736952.2:n.1136_1137insAA
NM_000748.3:c.884_885insAA MANE Select	NP_000739.1:p.Leu296SerfsTer?