Canonical Allele Identifier: CA342630229
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543825T>C (hg19) chr1:g.154571349T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571349T>C , CM000663.2:g.154571349T>C GRCh38
NC_000001.10:g.154543825T>C , CM000663.1:g.154543825T>C GRCh37
NC_000001.9:g.152810449T>C NCBI36
NG_008027.1:g.8569T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.526T>C MANE Select ENSP00000357461.3:p.Trp176Arg
ENST00000636034.1:c.526T>C ENSP00000489703.1:p.Trp176Arg
ENST00000637900.1:c.532T>C ENSP00000490474.1:p.Trp178Arg
ENST00000368476.3:c.526T>C ENSP00000357461.3:p.Trp176Arg
NM_000748.2:c.526T>C NP_000739.1:p.Trp176Arg
XM_017000180.2:c.16T>C XP_016855669.1:p.Trp6Arg
XR_001736952.2:n.778T>C
NM_000748.3:c.526T>C MANE Select NP_000739.1:p.Trp176Arg
Search 100 bp 5'
Search 100 bp 3'