Canonical Allele Identifier: CA2648172975
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154576053-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576053T>G , CM000663.2:g.154576053T>G GRCh38
NC_000001.10:g.154548529T>G , CM000663.1:g.154548529T>G GRCh37
NC_000001.9:g.152815153T>G NCBI36
NG_008027.1:g.13273T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*121T>G MANE Select ENSP00000357461.3:n.*121T>G
ENST00000636034.1:c.1505+125T>G ENSP00000489703.1:n.1505+125T>G
ENST00000637900.1:c.*121T>G ENSP00000490474.1:n.*121T>G
ENST00000368476.3:c.*121T>G ENSP00000357461.3:n.*121T>G
NM_000748.2:c.*121T>G NP_000739.1:n.*121T>G
XM_017000180.2:c.*121T>G XP_016855669.1:n.*121T>G
XR_001736952.2:n.1882T>G
NM_000748.3:c.*121T>G MANE Select NP_000739.1:n.*121T>G
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