Canonical Allele Identifier: CA342631042
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544186T>A (hg19) chr1:g.154571710T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571710T>A , CM000663.2:g.154571710T>A GRCh38
NC_000001.10:g.154544186T>A , CM000663.1:g.154544186T>A GRCh37
NC_000001.9:g.152810810T>A NCBI36
NG_008027.1:g.8930T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.887T>A MANE Select ENSP00000357461.3:p.Leu296His
ENST00000636034.1:c.887T>A ENSP00000489703.1:p.Leu296His
ENST00000637900.1:c.893T>A ENSP00000490474.1:p.Leu298His
ENST00000368476.3:c.887T>A ENSP00000357461.3:p.Leu296His
NM_000748.2:c.887T>A NP_000739.1:p.Leu296His
XM_017000180.2:c.377T>A XP_016855669.1:p.Leu126His
XR_001736952.2:n.1139T>A
NM_000748.3:c.887T>A MANE Select NP_000739.1:p.Leu296His
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