Canonical Allele Identifier: CA342630134
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543784T>G (hg19) chr1:g.154571308T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571308T>G , CM000663.2:g.154571308T>G GRCh38
NC_000001.10:g.154543784T>G , CM000663.1:g.154543784T>G GRCh37
NC_000001.9:g.152810408T>G NCBI36
NG_008027.1:g.8528T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.485T>G MANE Select ENSP00000357461.3:p.Phe162Cys
ENST00000636034.1:c.485T>G ENSP00000489703.1:p.Phe162Cys
ENST00000637900.1:c.491T>G ENSP00000490474.1:p.Phe164Cys
ENST00000368476.3:c.485T>G ENSP00000357461.3:p.Phe162Cys
NM_000748.2:c.485T>G NP_000739.1:p.Phe162Cys
XM_017000180.2:c.-9-17T>G XP_016855669.1:n.-9-17T>G
XR_001736952.2:n.737T>G
NM_000748.3:c.485T>G MANE Select NP_000739.1:p.Phe162Cys
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