Canonical Allele Identifier: CA1007940639
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs2149366079
gnomAD v3: 1-154569385-C-A
gnomAD v4: 1-154569385-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154569385C>A , CM000663.2:g.154569385C>A GRCh38
NC_000001.10:g.154541861C>A , CM000663.1:g.154541861C>A GRCh37
NC_000001.9:g.152808485C>A NCBI36
NG_008027.1:g.6605C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.65-77C>A MANE Select ENSP00000357461.3:n.65-77C>A
ENST00000636034.1:c.65-77C>A ENSP00000489703.1:n.65-77C>A
ENST00000637900.1:c.65-77C>A ENSP00000490474.1:n.65-77C>A
ENST00000368476.3:c.65-77C>A ENSP00000357461.3:n.65-77C>A
NM_000748.2:c.65-77C>A NP_000739.1:n.65-77C>A
XM_017000180.2:c.-310-77C>A XP_016855669.1:n.-310-77C>A
XR_001736952.2:n.317-77C>A
NM_000748.3:c.65-77C>A MANE Select NP_000739.1:n.65-77C>A
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