Canonical Allele Identifier: CA342631157
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544243G>A (hg19) chr1:g.154571767G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571767G>A , CM000663.2:g.154571767G>A GRCh38
NC_000001.10:g.154544243G>A , CM000663.1:g.154544243G>A GRCh37
NC_000001.9:g.152810867G>A NCBI36
NG_008027.1:g.8987G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.944G>A MANE Select ENSP00000357461.3:p.Ser315Asn
ENST00000636034.1:c.944G>A ENSP00000489703.1:p.Ser315Asn
ENST00000637900.1:c.950G>A ENSP00000490474.1:p.Ser317Asn
ENST00000368476.3:c.944G>A ENSP00000357461.3:p.Ser315Asn
NM_000748.2:c.944G>A NP_000739.1:p.Ser315Asn
XM_017000180.2:c.434G>A XP_016855669.1:p.Ser145Asn
XR_001736952.2:n.1196G>A
NM_000748.3:c.944G>A MANE Select NP_000739.1:p.Ser315Asn
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