Canonical Allele Identifier: CA397802006
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7359112G>C (hg19) chr17:g.7455793G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455793G>C , CM000679.2:g.7455793G>C GRCh38
NC_000017.10:g.7359112G>C , CM000679.1:g.7359112G>C GRCh37
NC_000017.9:g.7299836G>C NCBI36
NG_008026.1:g.15707G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.1218-1G>C MANE Select ENSP00000304290.2:n.1218-1G>C
ENST00000306071.6:c.1218-1G>C ENSP00000304290.2:n.1218-1G>C
ENST00000536404.6:c.1002-1G>C ENSP00000439209.2:n.1002-1G>C
ENST00000570557.5:c.881-1G>C
ENST00000575379.1:c.-176G>C ENSP00000461751.1:n.-176G>C
ENST00000576360.1:c.855-1G>C ENSP00000459092.1:n.855-1G>C
NM_000747.2:c.1218-1G>C NP_000738.2:n.1218-1G>C
NM_000747.3:c.1218-1G>C MANE Select NP_000738.2:n.1218-1G>C
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