Canonical Allele Identifier: CA342630999
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1571022383
MyVariant Identifiers: chr1:g.154544167A>C (hg19) chr1:g.154571691A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571691A>C , CM000663.2:g.154571691A>C GRCh38
NC_000001.10:g.154544167A>C , CM000663.1:g.154544167A>C GRCh37
NC_000001.9:g.152810791A>C NCBI36
NG_008027.1:g.8911A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.868A>C MANE Select ENSP00000357461.3:p.Thr290Pro
ENST00000636034.1:c.868A>C ENSP00000489703.1:p.Thr290Pro
ENST00000637900.1:c.874A>C ENSP00000490474.1:p.Thr292Pro
ENST00000368476.3:c.868A>C ENSP00000357461.3:p.Thr290Pro
NM_000748.2:c.868A>C NP_000739.1:p.Thr290Pro
XM_017000180.2:c.358A>C XP_016855669.1:p.Thr120Pro
XR_001736952.2:n.1120A>C
NM_000748.3:c.868A>C MANE Select NP_000739.1:p.Thr290Pro
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