Canonical Allele Identifier: CA371102541

Gene: CHRNB3

Linked Data

• MyVariant Identifiers: chr8:g.42587667T>A (hg19) ; chr8:g.42732524T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732524T>A , CM000670.2:g.42732524T>A	GRCh38
NC_000008.10:g.42587667T>A , CM000670.1:g.42587667T>A	GRCh37
NC_000008.9:g.42706824T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1217T>A MANE Select	ENSP00000289957.2:p.Val406Glu
ENST00000289957.2:c.1217T>A	ENSP00000289957.2:p.Val406Glu
NM_000749.3:c.1217T>A	NP_000740.1:p.Val406Glu
XM_011544390.1:c.830T>A	XP_011542692.1:p.Val277Glu
NM_000749.4:c.1217T>A	NP_000740.1:p.Val406Glu
NM_001347717.1:c.995T>A	NP_001334646.1:p.Val332Glu
XM_011544390.2:c.830T>A	XP_011542692.1:p.Val277Glu
NM_000749.5:c.1217T>A MANE Select	NP_000740.1:p.Val406Glu
NM_001347717.2:c.995T>A	NP_001334646.1:p.Val332Glu