Canonical Allele Identifier: CA397797860

Gene: CHRNB1

Linked Data

• MyVariant Identifiers: chr17:g.7357720A>G (hg19) ; chr17:g.7454401A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454401A>G , CM000679.2:g.7454401A>G	GRCh38
NC_000017.10:g.7357720A>G , CM000679.1:g.7357720A>G	GRCh37
NC_000017.9:g.7298444A>G	NCBI36
NG_008026.1:g.14315A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.925A>G MANE Select	ENSP00000304290.2:p.Ile309Val
ENST00000306071.6:c.925A>G	ENSP00000304290.2:p.Ile309Val
ENST00000536404.6:c.709A>G	ENSP00000439209.2:p.Ile237Val
ENST00000570557.5:c.588A>G
ENST00000573209.1:n.1869A>G
ENST00000576360.1:c.605-43A>G	ENSP00000459092.1:n.605-43A>G
NM_000747.2:c.925A>G	NP_000738.2:p.Ile309Val
NM_000747.3:c.925A>G MANE Select	NP_000738.2:p.Ile309Val