Canonical Allele Identifier: CA30834624
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs950226631
MyVariant Identifiers: chr1:g.154544156T>G (hg19) chr1:g.154571680T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571680T>G , CM000663.2:g.154571680T>G GRCh38
NC_000001.10:g.154544156T>G , CM000663.1:g.154544156T>G GRCh37
NC_000001.9:g.152810780T>G NCBI36
NG_008027.1:g.8900T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.857T>G MANE Select ENSP00000357461.3:p.Ile286Ser
ENST00000636034.1:c.857T>G ENSP00000489703.1:p.Ile286Ser
ENST00000637900.1:c.863T>G ENSP00000490474.1:p.Ile288Ser
ENST00000368476.3:c.857T>G ENSP00000357461.3:p.Ile286Ser
NM_000748.2:c.857T>G NP_000739.1:p.Ile286Ser
XM_017000180.2:c.347T>G XP_016855669.1:p.Ile116Ser
XR_001736952.2:n.1109T>G
NM_000748.3:c.857T>G MANE Select NP_000739.1:p.Ile286Ser
Search 100 bp 5'
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