Canonical Allele Identifier: CA342630228
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543823C>A (hg19) chr1:g.154571347C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571347C>A , CM000663.2:g.154571347C>A GRCh38
NC_000001.10:g.154543823C>A , CM000663.1:g.154543823C>A GRCh37
NC_000001.9:g.152810447C>A NCBI36
NG_008027.1:g.8567C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.524C>A MANE Select ENSP00000357461.3:p.Ser175Ter
ENST00000636034.1:c.524C>A ENSP00000489703.1:p.Ser175Ter
ENST00000637900.1:c.530C>A ENSP00000490474.1:p.Ser177Ter
ENST00000368476.3:c.524C>A ENSP00000357461.3:p.Ser175Ter
NM_000748.2:c.524C>A NP_000739.1:p.Ser175Ter
XM_017000180.2:c.14C>A XP_016855669.1:p.Ser5Ter
XR_001736952.2:n.776C>A
NM_000748.3:c.524C>A MANE Select NP_000739.1:p.Ser175Ter
Search 100 bp 5'
Search 100 bp 3'