Canonical Allele Identifier: CA397797753
Gene: CHRNB1 HGNC NCBI

Linked Data

gnomAD v4: 17-7454395-A-G
MyVariant Identifiers: chr17:g.7357714A>G (hg19) chr17:g.7454395A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454395A>G , CM000679.2:g.7454395A>G GRCh38
NC_000017.10:g.7357714A>G , CM000679.1:g.7357714A>G GRCh37
NC_000017.9:g.7298438A>G NCBI36
NG_008026.1:g.14309A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.919A>G MANE Select ENSP00000304290.2:p.Ile307Val
ENST00000306071.6:c.919A>G ENSP00000304290.2:p.Ile307Val
ENST00000536404.6:c.703A>G ENSP00000439209.2:p.Ile235Val
ENST00000570557.5:c.582A>G
ENST00000573209.1:n.1863A>G
ENST00000576360.1:c.605-49A>G ENSP00000459092.1:n.605-49A>G
NM_000747.2:c.919A>G NP_000738.2:p.Ile307Val
NM_000747.3:c.919A>G MANE Select NP_000738.2:p.Ile307Val
Search 100 bp 5'
Search 100 bp 3'