Canonical Allele Identifier: CA342630910
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544120T>A (hg19) chr1:g.154571644T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571644T>A , CM000663.2:g.154571644T>A GRCh38
NC_000001.10:g.154544120T>A , CM000663.1:g.154544120T>A GRCh37
NC_000001.9:g.152810744T>A NCBI36
NG_008027.1:g.8864T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.821T>A MANE Select ENSP00000357461.3:p.Leu274Gln
ENST00000636034.1:c.821T>A ENSP00000489703.1:p.Leu274Gln
ENST00000637900.1:c.827T>A ENSP00000490474.1:p.Leu276Gln
ENST00000368476.3:c.821T>A ENSP00000357461.3:p.Leu274Gln
NM_000748.2:c.821T>A NP_000739.1:p.Leu274Gln
XM_017000180.2:c.311T>A XP_016855669.1:p.Leu104Gln
XR_001736952.2:n.1073T>A
NM_000748.3:c.821T>A MANE Select NP_000739.1:p.Leu274Gln
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