Canonical Allele Identifier: CA397800743
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7358670C>G (hg19) chr17:g.7455351C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455351C>G , CM000679.2:g.7455351C>G GRCh38
NC_000017.10:g.7358670C>G , CM000679.1:g.7358670C>G GRCh37
NC_000017.9:g.7299394C>G NCBI36
NG_008026.1:g.15265C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1112C>G MANE Select ENSP00000304290.2:p.Pro371Arg
ENST00000306071.6:c.1112C>G ENSP00000304290.2:p.Pro371Arg
ENST00000536404.6:c.896C>G ENSP00000439209.2:p.Pro299Arg
ENST00000570557.5:c.775C>G
ENST00000573209.1:n.2056C>G
ENST00000576360.1:c.749C>G ENSP00000459092.1:p.Pro250Arg
NM_000747.2:c.1112C>G NP_000738.2:p.Pro371Arg
NM_000747.3:c.1112C>G MANE Select NP_000738.2:p.Pro371Arg
Search 100 bp 5'
Search 100 bp 3'