Canonical Allele Identifier: CA497744774
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7358665G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455346G>C , CM000679.2:g.7455346G>C GRCh38
NC_000017.10:g.7358665G>C , CM000679.1:g.7358665G>C GRCh37
NC_000017.9:g.7299389G>C NCBI36
NG_008026.1:g.15260G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1107G>C MANE Select ENSP00000304290.2:p.Leu369=
ENST00000306071.6:c.1107G>C ENSP00000304290.2:p.Leu369=
ENST00000536404.6:c.891G>C ENSP00000439209.2:p.Leu297=
ENST00000570557.5:c.770G>C
ENST00000573209.1:n.2051G>C
ENST00000576360.1:c.744G>C ENSP00000459092.1:p.Leu248=
NM_000747.2:c.1107G>C NP_000738.2:p.Leu369=
NM_000747.3:c.1107G>C MANE Select NP_000738.2:p.Leu369=
Search 100 bp 5'
Search 100 bp 3'