Canonical Allele Identifier: CA342630754
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544048C>A (hg19) chr1:g.154571572C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571572C>A , CM000663.2:g.154571572C>A GRCh38
NC_000001.10:g.154544048C>A , CM000663.1:g.154544048C>A GRCh37
NC_000001.9:g.152810672C>A NCBI36
NG_008027.1:g.8792C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.749C>A MANE Select ENSP00000357461.3:p.Ser250Ter
ENST00000636034.1:c.749C>A ENSP00000489703.1:p.Ser250Ter
ENST00000637900.1:c.755C>A ENSP00000490474.1:p.Ser252Ter
ENST00000368476.3:c.749C>A ENSP00000357461.3:p.Ser250Ter
NM_000748.2:c.749C>A NP_000739.1:p.Ser250Ter
XM_017000180.2:c.239C>A XP_016855669.1:p.Ser80Ter
XR_001736952.2:n.1001C>A
NM_000748.3:c.749C>A MANE Select NP_000739.1:p.Ser250Ter
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