Canonical Allele Identifier: CA371102555

Gene: CHRNB3

Linked Data

• dbSNP Id: rs1402840534
• gnomAD v4: 8-42732530-A-G
• MyVariant Identifiers: chr8:g.42587673A>G (hg19) ; chr8:g.42732530A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732530A>G , CM000670.2:g.42732530A>G	GRCh38
NC_000008.10:g.42587673A>G , CM000670.1:g.42587673A>G	GRCh37
NC_000008.9:g.42706830A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1223A>G MANE Select	ENSP00000289957.2:p.Lys408Arg
ENST00000289957.2:c.1223A>G	ENSP00000289957.2:p.Lys408Arg
NM_000749.3:c.1223A>G	NP_000740.1:p.Lys408Arg
XM_011544390.1:c.836A>G	XP_011542692.1:p.Lys279Arg
NM_000749.4:c.1223A>G	NP_000740.1:p.Lys408Arg
NM_001347717.1:c.1001A>G	NP_001334646.1:p.Lys334Arg
XM_011544390.2:c.836A>G	XP_011542692.1:p.Lys279Arg
NM_000749.5:c.1223A>G MANE Select	NP_000740.1:p.Lys408Arg
NM_001347717.2:c.1001A>G	NP_001334646.1:p.Lys334Arg