Canonical Allele Identifier: CA342631067
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154571723-C-A
MyVariant Identifiers: chr1:g.154544199C>A (hg19) chr1:g.154571723C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571723C>A , CM000663.2:g.154571723C>A GRCh38
NC_000001.10:g.154544199C>A , CM000663.1:g.154544199C>A GRCh37
NC_000001.9:g.152810823C>A NCBI36
NG_008027.1:g.8943C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.900C>A MANE Select ENSP00000357461.3:p.Tyr300Ter
ENST00000636034.1:c.900C>A ENSP00000489703.1:p.Tyr300Ter
ENST00000637900.1:c.906C>A ENSP00000490474.1:p.Tyr302Ter
ENST00000368476.3:c.900C>A ENSP00000357461.3:p.Tyr300Ter
NM_000748.2:c.900C>A NP_000739.1:p.Tyr300Ter
XM_017000180.2:c.390C>A XP_016855669.1:p.Tyr130Ter
XR_001736952.2:n.1152C>A
NM_000748.3:c.900C>A MANE Select NP_000739.1:p.Tyr300Ter
Search 100 bp 5'
Search 100 bp 3'