Canonical Allele Identifier: CA342631038

Gene: CHRNB2

Linked Data

• gnomAD v4: 1-154571709-C-G
• MyVariant Identifiers: chr1:g.154544185C>G (hg19) ; chr1:g.154571709C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571709C>G , CM000663.2:g.154571709C>G	GRCh38
NC_000001.10:g.154544185C>G , CM000663.1:g.154544185C>G	GRCh37
NC_000001.9:g.152810809C>G	NCBI36
NG_008027.1:g.8929C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.886C>G MANE Select	ENSP00000357461.3:p.Leu296Val
ENST00000636034.1:c.886C>G	ENSP00000489703.1:p.Leu296Val
ENST00000637900.1:c.892C>G	ENSP00000490474.1:p.Leu298Val
ENST00000368476.3:c.886C>G	ENSP00000357461.3:p.Leu296Val
NM_000748.2:c.886C>G	NP_000739.1:p.Leu296Val
XM_017000180.2:c.376C>G	XP_016855669.1:p.Leu126Val
XR_001736952.2:n.1138C>G
NM_000748.3:c.886C>G MANE Select	NP_000739.1:p.Leu296Val