Canonical Allele Identifier: CA342630141
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543787C>G (hg19) chr1:g.154571311C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571311C>G , CM000663.2:g.154571311C>G GRCh38
NC_000001.10:g.154543787C>G , CM000663.1:g.154543787C>G GRCh37
NC_000001.9:g.152810411C>G NCBI36
NG_008027.1:g.8531C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.488C>G MANE Select ENSP00000357461.3:p.Pro163Arg
ENST00000636034.1:c.488C>G ENSP00000489703.1:p.Pro163Arg
ENST00000637900.1:c.494C>G ENSP00000490474.1:p.Pro165Arg
ENST00000368476.3:c.488C>G ENSP00000357461.3:p.Pro163Arg
NM_000748.2:c.488C>G NP_000739.1:p.Pro163Arg
XM_017000180.2:c.-9-14C>G XP_016855669.1:n.-9-14C>G
XR_001736952.2:n.740C>G
NM_000748.3:c.488C>G MANE Select NP_000739.1:p.Pro163Arg
Search 100 bp 5'
Search 100 bp 3'