Canonical Allele Identifier: CA526666203
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v2: 1-154544180-TGC-T
gnomAD v4: 1-154571704-TGC-T
MyVariant Identifiers: chr1:g.154544181_154544182del (hg19) chr1:g.154571705_154571706del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571705_154571706del , CM000663.2:g.154571705_154571706del GRCh38
NC_000001.10:g.154544181_154544182del , CM000663.1:g.154544181_154544182del GRCh37
NC_000001.9:g.152810805_152810806del NCBI36
NG_008027.1:g.8925_8926del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.882_883del MANE Select ENSP00000357461.3:p.Pro295AlafsTer?
ENST00000636034.1:c.882_883del ENSP00000489703.1:p.Pro295AlafsTer?
ENST00000637900.1:c.888_889del ENSP00000490474.1:p.Pro297AlafsTer?
ENST00000368476.3:c.882_883del ENSP00000357461.3:p.Pro295AlafsTer?
NM_000748.2:c.882_883del NP_000739.1:p.Pro295AlafsTer?
XM_017000180.2:c.372_373del XP_016855669.1:p.Pro125AlafsTer?
XR_001736952.2:n.1134_1135del
NM_000748.3:c.882_883del MANE Select NP_000739.1:p.Pro295AlafsTer?
Search 100 bp 5'
Search 100 bp 3'