Canonical Allele Identifier: CA342630813
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544077T>A (hg19) chr1:g.154571601T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571601T>A , CM000663.2:g.154571601T>A GRCh38
NC_000001.10:g.154544077T>A , CM000663.1:g.154544077T>A GRCh37
NC_000001.9:g.152810701T>A NCBI36
NG_008027.1:g.8821T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.778T>A MANE Select ENSP00000357461.3:p.Ser260Thr
ENST00000636034.1:c.778T>A ENSP00000489703.1:p.Ser260Thr
ENST00000637900.1:c.784T>A ENSP00000490474.1:p.Ser262Thr
ENST00000368476.3:c.778T>A ENSP00000357461.3:p.Ser260Thr
NM_000748.2:c.778T>A NP_000739.1:p.Ser260Thr
XM_017000180.2:c.268T>A XP_016855669.1:p.Ser90Thr
XR_001736952.2:n.1030T>A
NM_000748.3:c.778T>A MANE Select NP_000739.1:p.Ser260Thr
Search 100 bp 5'
Search 100 bp 3'