Canonical Allele Identifier: CA397800535

Gene: CHRNB1

Linked Data

• MyVariant Identifiers: chr17:g.7358645C>G (hg19) ; chr17:g.7455326C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455326C>G , CM000679.2:g.7455326C>G	GRCh38
NC_000017.10:g.7358645C>G , CM000679.1:g.7358645C>G	GRCh37
NC_000017.9:g.7299369C>G	NCBI36
NG_008026.1:g.15240C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1087C>G MANE Select	ENSP00000304290.2:p.Pro363Ala
ENST00000306071.6:c.1087C>G	ENSP00000304290.2:p.Pro363Ala
ENST00000536404.6:c.871C>G	ENSP00000439209.2:p.Pro291Ala
ENST00000570557.5:c.750C>G
ENST00000573209.1:n.2031C>G
ENST00000576360.1:c.724C>G	ENSP00000459092.1:p.Pro242Ala
NM_000747.2:c.1087C>G	NP_000738.2:p.Pro363Ala
NM_000747.3:c.1087C>G MANE Select	NP_000738.2:p.Pro363Ala