Canonical Allele Identifier: CA371102578

Gene: CHRNB3

Linked Data

• MyVariant Identifiers: chr8:g.42587682T>A (hg19) ; chr8:g.42732539T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732539T>A , CM000670.2:g.42732539T>A	GRCh38
NC_000008.10:g.42587682T>A , CM000670.1:g.42587682T>A	GRCh37
NC_000008.9:g.42706839T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1232T>A MANE Select	ENSP00000289957.2:p.Phe411Tyr
ENST00000289957.2:c.1232T>A	ENSP00000289957.2:p.Phe411Tyr
NM_000749.3:c.1232T>A	NP_000740.1:p.Phe411Tyr
XM_011544390.1:c.845T>A	XP_011542692.1:p.Phe282Tyr
NM_000749.4:c.1232T>A	NP_000740.1:p.Phe411Tyr
NM_001347717.1:c.1010T>A	NP_001334646.1:p.Phe337Tyr
XM_011544390.2:c.845T>A	XP_011542692.1:p.Phe282Tyr
NM_000749.5:c.1232T>A MANE Select	NP_000740.1:p.Phe411Tyr
NM_001347717.2:c.1010T>A	NP_001334646.1:p.Phe337Tyr