Canonical Allele Identifier: CA421231268
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544181G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571705G>C , CM000663.2:g.154571705G>C GRCh38
NC_000001.10:g.154544181G>C , CM000663.1:g.154544181G>C GRCh37
NC_000001.9:g.152810805G>C NCBI36
NG_008027.1:g.8925G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.882G>C MANE Select ENSP00000357461.3:p.Val294=
ENST00000636034.1:c.882G>C ENSP00000489703.1:p.Val294=
ENST00000637900.1:c.888G>C ENSP00000490474.1:p.Val296=
ENST00000368476.3:c.882G>C ENSP00000357461.3:p.Val294=
NM_000748.2:c.882G>C NP_000739.1:p.Val294=
XM_017000180.2:c.372G>C XP_016855669.1:p.Val124=
XR_001736952.2:n.1134G>C
NM_000748.3:c.882G>C MANE Select NP_000739.1:p.Val294=
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