Canonical Allele Identifier: CA774956928

Gene: CHRNB1

Linked Data

• dbSNP Id: rs1489911996
• gnomAD v3: 17-7454579-A-G
• gnomAD v4: 17-7454579-A-G
• MyVariant Identifiers: chr17:g.7357898A>G (hg19) ; chr17:g.7454579A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454579A>G , CM000679.2:g.7454579A>G	GRCh38
NC_000017.10:g.7357898A>G , CM000679.1:g.7357898A>G	GRCh37
NC_000017.9:g.7298622A>G	NCBI36
NG_008026.1:g.14493A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1044+59A>G MANE Select	ENSP00000304290.2:n.1044+59A>G
ENST00000306071.6:c.1044+59A>G	ENSP00000304290.2:n.1044+59A>G
ENST00000536404.6:c.828+59A>G	ENSP00000439209.2:n.828+59A>G
ENST00000570557.5:c.707+59A>G
ENST00000573209.1:n.1988+59A>G
ENST00000576360.1:c.681+59A>G	ENSP00000459092.1:n.681+59A>G
NM_000747.2:c.1044+59A>G	NP_000738.2:n.1044+59A>G
NM_000747.3:c.1044+59A>G MANE Select	NP_000738.2:n.1044+59A>G