Canonical Allele Identifier: CA397798028

Gene: CHRNB1

Linked Data

• MyVariant Identifiers: chr17:g.7357737T>G (hg19) ; chr17:g.7454418T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454418T>G , CM000679.2:g.7454418T>G	GRCh38
NC_000017.10:g.7357737T>G , CM000679.1:g.7357737T>G	GRCh37
NC_000017.9:g.7298461T>G	NCBI36
NG_008026.1:g.14332T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.942T>G MANE Select	ENSP00000304290.2:p.Phe314Leu
ENST00000306071.6:c.942T>G	ENSP00000304290.2:p.Phe314Leu
ENST00000536404.6:c.726T>G	ENSP00000439209.2:p.Phe242Leu
ENST00000570557.5:c.605T>G
ENST00000573209.1:n.1886T>G
ENST00000576360.1:c.605-26T>G	ENSP00000459092.1:n.605-26T>G
NM_000747.2:c.942T>G	NP_000738.2:p.Phe314Leu
NM_000747.3:c.942T>G MANE Select	NP_000738.2:p.Phe314Leu