Canonical Allele Identifier: CA421231321
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs748080172
gnomAD v2: 1-154544211-C-T
gnomAD v4: 1-154571735-C-T
MyVariant Identifiers: chr1:g.154544211C>T (hg19) chr1:g.154571735C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571735C>T , CM000663.2:g.154571735C>T GRCh38
NC_000001.10:g.154544211C>T , CM000663.1:g.154544211C>T GRCh37
NC_000001.9:g.152810835C>T NCBI36
NG_008027.1:g.8955C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.912C>T MANE Select ENSP00000357461.3:p.Thr304=
ENST00000636034.1:c.912C>T ENSP00000489703.1:p.Thr304=
ENST00000637900.1:c.918C>T ENSP00000490474.1:p.Thr306=
ENST00000368476.3:c.912C>T ENSP00000357461.3:p.Thr304=
NM_000748.2:c.912C>T NP_000739.1:p.Thr304=
XM_017000180.2:c.402C>T XP_016855669.1:p.Thr134=
XR_001736952.2:n.1164C>T
NM_000748.3:c.912C>T MANE Select NP_000739.1:p.Thr304=
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