Canonical Allele Identifier: CA2648173689
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154571182-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571182T>G , CM000663.2:g.154571182T>G GRCh38
NC_000001.10:g.154543658T>G , CM000663.1:g.154543658T>G GRCh37
NC_000001.9:g.152810282T>G NCBI36
NG_008027.1:g.8402T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.366-7T>G MANE Select ENSP00000357461.3:n.366-7T>G
ENST00000636034.1:c.366-7T>G ENSP00000489703.1:n.366-7T>G
ENST00000637900.1:c.372-7T>G ENSP00000490474.1:n.372-7T>G
ENST00000368476.3:c.366-7T>G ENSP00000357461.3:n.366-7T>G
NM_000748.2:c.366-7T>G NP_000739.1:n.366-7T>G
XM_017000180.2:c.-9-143T>G XP_016855669.1:n.-9-143T>G
XR_001736952.2:n.618-7T>G
NM_000748.3:c.366-7T>G MANE Select NP_000739.1:n.366-7T>G
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