Canonical Allele Identifier: CA1130735
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs538508561
ExAC: 1:154543758 C / G
gnomAD v2: 1-154543758-C-G
gnomAD v4: 1-154571282-C-G
MyVariant Identifiers: chr1:g.154543758C>G (hg19) chr1:g.154571282C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571282C>G , CM000663.2:g.154571282C>G GRCh38
NC_000001.10:g.154543758C>G , CM000663.1:g.154543758C>G GRCh37
NC_000001.9:g.152810382C>G NCBI36
NG_008027.1:g.8502C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.459C>G MANE Select ENSP00000357461.3:p.Ser153Arg
ENST00000636034.1:c.459C>G ENSP00000489703.1:p.Ser153Arg
ENST00000637900.1:c.465C>G ENSP00000490474.1:p.Ser155Arg
ENST00000368476.3:c.459C>G ENSP00000357461.3:p.Ser153Arg
NM_000748.2:c.459C>G NP_000739.1:p.Ser153Arg
XM_017000180.2:c.-9-43C>G XP_016855669.1:n.-9-43C>G
XR_001736952.2:n.711C>G
NM_000748.3:c.459C>G MANE Select NP_000739.1:p.Ser153Arg
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