Canonical Allele Identifier: CA421231227
Gene: CHRNB2 HGNC NCBI

Linked Data

COSMIC: COSM4672283
MyVariant Identifiers: chr1:g.154544160G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571684G>A , CM000663.2:g.154571684G>A GRCh38
NC_000001.10:g.154544160G>A , CM000663.1:g.154544160G>A GRCh37
NC_000001.9:g.152810784G>A NCBI36
NG_008027.1:g.8904G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.861G>A MANE Select ENSP00000357461.3:p.Val287=
ENST00000636034.1:c.861G>A ENSP00000489703.1:p.Val287=
ENST00000637900.1:c.867G>A ENSP00000490474.1:p.Val289=
ENST00000368476.3:c.861G>A ENSP00000357461.3:p.Val287=
NM_000748.2:c.861G>A NP_000739.1:p.Val287=
XM_017000180.2:c.351G>A XP_016855669.1:p.Val117=
XR_001736952.2:n.1113G>A
NM_000748.3:c.861G>A MANE Select NP_000739.1:p.Val287=
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