Canonical Allele Identifier: CA371102588

Gene: CHRNB3

Linked Data

• MyVariant Identifiers: chr8:g.42587686C>G (hg19) ; chr8:g.42732543C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732543C>G , CM000670.2:g.42732543C>G	GRCh38
NC_000008.10:g.42587686C>G , CM000670.1:g.42587686C>G	GRCh37
NC_000008.9:g.42706843C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1236C>G MANE Select	ENSP00000289957.2:p.Ile412Met
ENST00000289957.2:c.1236C>G	ENSP00000289957.2:p.Ile412Met
NM_000749.3:c.1236C>G	NP_000740.1:p.Ile412Met
XM_011544390.1:c.849C>G	XP_011542692.1:p.Ile283Met
NM_000749.4:c.1236C>G	NP_000740.1:p.Ile412Met
NM_001347717.1:c.1014C>G	NP_001334646.1:p.Ile338Met
XM_011544390.2:c.849C>G	XP_011542692.1:p.Ile283Met
NM_000749.5:c.1236C>G MANE Select	NP_000740.1:p.Ile412Met
NM_001347717.2:c.1014C>G	NP_001334646.1:p.Ile338Met