Canonical Allele Identifier: CA342630871
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154571626-T-A
MyVariant Identifiers: chr1:g.154544102T>A (hg19) chr1:g.154571626T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571626T>A , CM000663.2:g.154571626T>A GRCh38
NC_000001.10:g.154544102T>A , CM000663.1:g.154544102T>A GRCh37
NC_000001.9:g.152810726T>A NCBI36
NG_008027.1:g.8846T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.803T>A MANE Select ENSP00000357461.3:p.Leu268Ter
ENST00000636034.1:c.803T>A ENSP00000489703.1:p.Leu268Ter
ENST00000637900.1:c.809T>A ENSP00000490474.1:p.Leu270Ter
ENST00000368476.3:c.803T>A ENSP00000357461.3:p.Leu268Ter
NM_000748.2:c.803T>A NP_000739.1:p.Leu268Ter
XM_017000180.2:c.293T>A XP_016855669.1:p.Leu98Ter
XR_001736952.2:n.1055T>A
NM_000748.3:c.803T>A MANE Select NP_000739.1:p.Leu268Ter
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