Canonical Allele Identifier: CA421231164
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544133C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571657C>G , CM000663.2:g.154571657C>G GRCh38
NC_000001.10:g.154544133C>G , CM000663.1:g.154544133C>G GRCh37
NC_000001.9:g.152810757C>G NCBI36
NG_008027.1:g.8877C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.834C>G MANE Select ENSP00000357461.3:p.Val278=
ENST00000636034.1:c.834C>G ENSP00000489703.1:p.Val278=
ENST00000637900.1:c.840C>G ENSP00000490474.1:p.Val280=
ENST00000368476.3:c.834C>G ENSP00000357461.3:p.Val278=
NM_000748.2:c.834C>G NP_000739.1:p.Val278=
XM_017000180.2:c.324C>G XP_016855669.1:p.Val108=
XR_001736952.2:n.1086C>G
NM_000748.3:c.834C>G MANE Select NP_000739.1:p.Val278=
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