Canonical Allele Identifier: CA526408569
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1220079950
gnomAD v2: 1-154548689-G-A
gnomAD v3: 1-154576213-G-A
gnomAD v4: 1-154576213-G-A
MyVariant Identifiers: chr1:g.154548689G>A (hg19) chr1:g.154576213G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576213G>A , CM000663.2:g.154576213G>A GRCh38
NC_000001.10:g.154548689G>A , CM000663.1:g.154548689G>A GRCh37
NC_000001.9:g.152815313G>A NCBI36
NG_008027.1:g.13433G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*281G>A MANE Select ENSP00000357461.3:n.*281G>A
ENST00000636034.1:c.1505+285G>A ENSP00000489703.1:n.1505+285G>A
ENST00000637900.1:c.*281G>A ENSP00000490474.1:n.*281G>A
ENST00000368476.3:c.*281G>A ENSP00000357461.3:n.*281G>A
NM_000748.2:c.*281G>A NP_000739.1:n.*281G>A
XM_017000180.2:c.*281G>A XP_016855669.1:n.*281G>A
XR_001736952.2:n.2042G>A
NM_000748.3:c.*281G>A MANE Select NP_000739.1:n.*281G>A
Search 100 bp 5'
Search 100 bp 3'