Canonical Allele Identifier: CA342630068
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543757G>A (hg19) chr1:g.154571281G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571281G>A , CM000663.2:g.154571281G>A GRCh38
NC_000001.10:g.154543757G>A , CM000663.1:g.154543757G>A GRCh37
NC_000001.9:g.152810381G>A NCBI36
NG_008027.1:g.8501G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.458G>A MANE Select ENSP00000357461.3:p.Ser153Asn
ENST00000636034.1:c.458G>A ENSP00000489703.1:p.Ser153Asn
ENST00000637900.1:c.464G>A ENSP00000490474.1:p.Ser155Asn
ENST00000368476.3:c.458G>A ENSP00000357461.3:p.Ser153Asn
NM_000748.2:c.458G>A NP_000739.1:p.Ser153Asn
XM_017000180.2:c.-9-44G>A XP_016855669.1:n.-9-44G>A
XR_001736952.2:n.710G>A
NM_000748.3:c.458G>A MANE Select NP_000739.1:p.Ser153Asn
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