Canonical Allele Identifier: CA460568677

Gene: CHRNB3

Linked Data

• MyVariant Identifiers: chr8:g.42587689C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732546C>T , CM000670.2:g.42732546C>T	GRCh38
NC_000008.10:g.42587689C>T , CM000670.1:g.42587689C>T	GRCh37
NC_000008.9:g.42706846C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1239C>T MANE Select	ENSP00000289957.2:p.Ser413=
ENST00000289957.2:c.1239C>T	ENSP00000289957.2:p.Ser413=
NM_000749.3:c.1239C>T	NP_000740.1:p.Ser413=
XM_011544390.1:c.852C>T	XP_011542692.1:p.Ser284=
NM_000749.4:c.1239C>T	NP_000740.1:p.Ser413=
NM_001347717.1:c.1017C>T	NP_001334646.1:p.Ser339=
XM_011544390.2:c.852C>T	XP_011542692.1:p.Ser284=
NM_000749.5:c.1239C>T MANE Select	NP_000740.1:p.Ser413=
NM_001347717.2:c.1017C>T	NP_001334646.1:p.Ser339=