Canonical Allele Identifier: CA342629879
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543671C>A (hg19) chr1:g.154571195C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571195C>A , CM000663.2:g.154571195C>A GRCh38
NC_000001.10:g.154543671C>A , CM000663.1:g.154543671C>A GRCh37
NC_000001.9:g.152810295C>A NCBI36
NG_008027.1:g.8415C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.372C>A MANE Select ENSP00000357461.3:p.Asp124Glu
ENST00000636034.1:c.372C>A ENSP00000489703.1:p.Asp124Glu
ENST00000637900.1:c.378C>A ENSP00000490474.1:p.Asp126Glu
ENST00000368476.3:c.372C>A ENSP00000357461.3:p.Asp124Glu
NM_000748.2:c.372C>A NP_000739.1:p.Asp124Glu
XM_017000180.2:c.-9-130C>A XP_016855669.1:n.-9-130C>A
XR_001736952.2:n.624C>A
NM_000748.3:c.372C>A MANE Select NP_000739.1:p.Asp124Glu
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