Canonical Allele Identifier: CA342630966
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154571673-T-A
MyVariant Identifiers: chr1:g.154544149T>A (hg19) chr1:g.154571673T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571673T>A , CM000663.2:g.154571673T>A GRCh38
NC_000001.10:g.154544149T>A , CM000663.1:g.154544149T>A GRCh37
NC_000001.9:g.152810773T>A NCBI36
NG_008027.1:g.8893T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.850T>A MANE Select ENSP00000357461.3:p.Ser284Thr
ENST00000636034.1:c.850T>A ENSP00000489703.1:p.Ser284Thr
ENST00000637900.1:c.856T>A ENSP00000490474.1:p.Ser286Thr
ENST00000368476.3:c.850T>A ENSP00000357461.3:p.Ser284Thr
NM_000748.2:c.850T>A NP_000739.1:p.Ser284Thr
XM_017000180.2:c.340T>A XP_016855669.1:p.Ser114Thr
XR_001736952.2:n.1102T>A
NM_000748.3:c.850T>A MANE Select NP_000739.1:p.Ser284Thr
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