Canonical Allele Identifier: CA2480925332
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571682_154571683delinsGT , CM000663.2:g.154571682_154571683delinsGT GRCh38
NC_000001.10:g.154544158_154544159delinsGT , CM000663.1:g.154544158_154544159delinsGT GRCh37
NC_000001.9:g.152810782_152810783delinsGT NCBI36
NG_008027.1:g.8902_8903delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.859_860delinsGT MANE Select ENSP00000357461.3:p.Val287=
ENST00000636034.1:c.859_860delinsGT ENSP00000489703.1:p.Val287=
ENST00000637900.1:c.865_866delinsGT ENSP00000490474.1:p.Val289=
ENST00000368476.3:c.859_860delinsGT ENSP00000357461.3:p.Val287=
NM_000748.2:c.859_860delinsGT NP_000739.1:p.Val287=
XM_017000180.2:c.349_350delinsGT XP_016855669.1:p.Val117=
XR_001736952.2:n.1111_1112delinsGT
NM_000748.3:c.859_860delinsGT MANE Select NP_000739.1:p.Val287=
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