Canonical Allele Identifier: CA397797732

Gene: CHRNB1

Linked Data

• MyVariant Identifiers: chr17:g.7357712C>T (hg19) ; chr17:g.7454393C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454393C>T , CM000679.2:g.7454393C>T	GRCh38
NC_000017.10:g.7357712C>T , CM000679.1:g.7357712C>T	GRCh37
NC_000017.9:g.7298436C>T	NCBI36
NG_008026.1:g.14307C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.917C>T MANE Select	ENSP00000304290.2:p.Pro306Leu
ENST00000306071.6:c.917C>T	ENSP00000304290.2:p.Pro306Leu
ENST00000536404.6:c.701C>T	ENSP00000439209.2:p.Pro234Leu
ENST00000570557.5:c.580C>T
ENST00000573209.1:n.1861C>T
ENST00000576360.1:c.605-51C>T	ENSP00000459092.1:n.605-51C>T
NM_000747.2:c.917C>T	NP_000738.2:p.Pro306Leu
NM_000747.3:c.917C>T MANE Select	NP_000738.2:p.Pro306Leu