Canonical Allele Identifier: CA342630928
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544131G>A (hg19) chr1:g.154571655G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571655G>A , CM000663.2:g.154571655G>A GRCh38
NC_000001.10:g.154544131G>A , CM000663.1:g.154544131G>A GRCh37
NC_000001.9:g.152810755G>A NCBI36
NG_008027.1:g.8875G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.832G>A MANE Select ENSP00000357461.3:p.Val278Ile
ENST00000636034.1:c.832G>A ENSP00000489703.1:p.Val278Ile
ENST00000637900.1:c.838G>A ENSP00000490474.1:p.Val280Ile
ENST00000368476.3:c.832G>A ENSP00000357461.3:p.Val278Ile
NM_000748.2:c.832G>A NP_000739.1:p.Val278Ile
XM_017000180.2:c.322G>A XP_016855669.1:p.Val108Ile
XR_001736952.2:n.1084G>A
NM_000748.3:c.832G>A MANE Select NP_000739.1:p.Val278Ile
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