Canonical Allele Identifier: CA342631179
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544252T>A (hg19) chr1:g.154571776T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571776T>A , CM000663.2:g.154571776T>A GRCh38
NC_000001.10:g.154544252T>A , CM000663.1:g.154544252T>A GRCh37
NC_000001.9:g.152810876T>A NCBI36
NG_008027.1:g.8996T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.953T>A MANE Select ENSP00000357461.3:p.Val318Glu
ENST00000636034.1:c.953T>A ENSP00000489703.1:p.Val318Glu
ENST00000637900.1:c.959T>A ENSP00000490474.1:p.Val320Glu
ENST00000368476.3:c.953T>A ENSP00000357461.3:p.Val318Glu
NM_000748.2:c.953T>A NP_000739.1:p.Val318Glu
XM_017000180.2:c.443T>A XP_016855669.1:p.Val148Glu
XR_001736952.2:n.1205T>A
NM_000748.3:c.953T>A MANE Select NP_000739.1:p.Val318Glu
Search 100 bp 5'
Search 100 bp 3'