Canonical Allele Identifier: CA342631034
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1455115470
MyVariant Identifiers: chr1:g.154544183C>A (hg19) chr1:g.154571707C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571707C>A , CM000663.2:g.154571707C>A GRCh38
NC_000001.10:g.154544183C>A , CM000663.1:g.154544183C>A GRCh37
NC_000001.9:g.152810807C>A NCBI36
NG_008027.1:g.8927C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.884C>A MANE Select ENSP00000357461.3:p.Pro295Gln
ENST00000636034.1:c.884C>A ENSP00000489703.1:p.Pro295Gln
ENST00000637900.1:c.890C>A ENSP00000490474.1:p.Pro297Gln
ENST00000368476.3:c.884C>A ENSP00000357461.3:p.Pro295Gln
NM_000748.2:c.884C>A NP_000739.1:p.Pro295Gln
XM_017000180.2:c.374C>A XP_016855669.1:p.Pro125Gln
XR_001736952.2:n.1136C>A
NM_000748.3:c.884C>A MANE Select NP_000739.1:p.Pro295Gln
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