Canonical Allele Identifier: CA2648173295
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154576166-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576166C>T , CM000663.2:g.154576166C>T GRCh38
NC_000001.10:g.154548642C>T , CM000663.1:g.154548642C>T GRCh37
NC_000001.9:g.152815266C>T NCBI36
NG_008027.1:g.13386C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*234C>T MANE Select ENSP00000357461.3:n.*234C>T
ENST00000636034.1:c.1505+238C>T ENSP00000489703.1:n.1505+238C>T
ENST00000637900.1:c.*234C>T ENSP00000490474.1:n.*234C>T
ENST00000368476.3:c.*234C>T ENSP00000357461.3:n.*234C>T
NM_000748.2:c.*234C>T NP_000739.1:n.*234C>T
XM_017000180.2:c.*234C>T XP_016855669.1:n.*234C>T
XR_001736952.2:n.1995C>T
NM_000748.3:c.*234C>T MANE Select NP_000739.1:n.*234C>T
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