Canonical Allele Identifier: CA342630867
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544099C>G (hg19) chr1:g.154571623C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571623C>G , CM000663.2:g.154571623C>G GRCh38
NC_000001.10:g.154544099C>G , CM000663.1:g.154544099C>G GRCh37
NC_000001.9:g.152810723C>G NCBI36
NG_008027.1:g.8843C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.800C>G MANE Select ENSP00000357461.3:p.Thr267Arg
ENST00000636034.1:c.800C>G ENSP00000489703.1:p.Thr267Arg
ENST00000637900.1:c.806C>G ENSP00000490474.1:p.Thr269Arg
ENST00000368476.3:c.800C>G ENSP00000357461.3:p.Thr267Arg
NM_000748.2:c.800C>G NP_000739.1:p.Thr267Arg
XM_017000180.2:c.290C>G XP_016855669.1:p.Thr97Arg
XR_001736952.2:n.1052C>G
NM_000748.3:c.800C>G MANE Select NP_000739.1:p.Thr267Arg
Search 100 bp 5'
Search 100 bp 3'