Canonical Allele Identifier: CA397802615

Gene: CHRNB1

Linked Data

• gnomAD v4: 17-7455879-G-T
• MyVariant Identifiers: chr17:g.7359198G>T (hg19) ; chr17:g.7455879G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455879G>T , CM000679.2:g.7455879G>T	GRCh38
NC_000017.10:g.7359198G>T , CM000679.1:g.7359198G>T	GRCh37
NC_000017.9:g.7299922G>T	NCBI36
NG_008026.1:g.15793G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1303G>T MANE Select	ENSP00000304290.2:p.Glu435Ter
ENST00000306071.6:c.1303G>T	ENSP00000304290.2:p.Glu435Ter
ENST00000536404.6:c.1087G>T	ENSP00000439209.2:p.Glu363Ter
ENST00000575379.1:c.-90G>T	ENSP00000461751.1:n.-90G>T
ENST00000576360.1:c.940G>T	ENSP00000459092.1:p.Glu314Ter
NM_000747.2:c.1303G>T	NP_000738.2:p.Glu435Ter
NM_000747.3:c.1303G>T MANE Select	NP_000738.2:p.Glu435Ter