Canonical Allele Identifier: CA342629918
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154571211-T-A
MyVariant Identifiers: chr1:g.154543687T>A (hg19) chr1:g.154571211T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571211T>A , CM000663.2:g.154571211T>A GRCh38
NC_000001.10:g.154543687T>A , CM000663.1:g.154543687T>A GRCh37
NC_000001.9:g.152810311T>A NCBI36
NG_008027.1:g.8431T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.388T>A MANE Select ENSP00000357461.3:p.Ser130Thr
ENST00000636034.1:c.388T>A ENSP00000489703.1:p.Ser130Thr
ENST00000637900.1:c.394T>A ENSP00000490474.1:p.Ser132Thr
ENST00000368476.3:c.388T>A ENSP00000357461.3:p.Ser130Thr
NM_000748.2:c.388T>A NP_000739.1:p.Ser130Thr
XM_017000180.2:c.-9-114T>A XP_016855669.1:n.-9-114T>A
XR_001736952.2:n.640T>A
NM_000748.3:c.388T>A MANE Select NP_000739.1:p.Ser130Thr
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