Canonical Allele Identifier: CA397801991
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7359111A>T (hg19) chr17:g.7455792A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455792A>T , CM000679.2:g.7455792A>T GRCh38
NC_000017.10:g.7359111A>T , CM000679.1:g.7359111A>T GRCh37
NC_000017.9:g.7299835A>T NCBI36
NG_008026.1:g.15706A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1218-2A>T MANE Select ENSP00000304290.2:n.1218-2A>T
ENST00000306071.6:c.1218-2A>T ENSP00000304290.2:n.1218-2A>T
ENST00000536404.6:c.1002-2A>T ENSP00000439209.2:n.1002-2A>T
ENST00000570557.5:c.881-2A>T
ENST00000575379.1:c.-177A>T ENSP00000461751.1:n.-177A>T
ENST00000576360.1:c.855-2A>T ENSP00000459092.1:n.855-2A>T
NM_000747.2:c.1218-2A>T NP_000738.2:n.1218-2A>T
NM_000747.3:c.1218-2A>T MANE Select NP_000738.2:n.1218-2A>T
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