Canonical Allele Identifier: CA342630219
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543818C>A (hg19) chr1:g.154571342C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571342C>A , CM000663.2:g.154571342C>A GRCh38
NC_000001.10:g.154543818C>A , CM000663.1:g.154543818C>A GRCh37
NC_000001.9:g.152810442C>A NCBI36
NG_008027.1:g.8562C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.519C>A MANE Select ENSP00000357461.3:p.Phe173Leu
ENST00000636034.1:c.519C>A ENSP00000489703.1:p.Phe173Leu
ENST00000637900.1:c.525C>A ENSP00000490474.1:p.Phe175Leu
ENST00000368476.3:c.519C>A ENSP00000357461.3:p.Phe173Leu
NM_000748.2:c.519C>A NP_000739.1:p.Phe173Leu
XM_017000180.2:c.9C>A XP_016855669.1:p.Phe3Leu
XR_001736952.2:n.771C>A
NM_000748.3:c.519C>A MANE Select NP_000739.1:p.Phe173Leu
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