Canonical Allele Identifier: CA2573911888
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154569391-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154569391C>G , CM000663.2:g.154569391C>G GRCh38
NC_000001.10:g.154541867C>G , CM000663.1:g.154541867C>G GRCh37
NC_000001.9:g.152808491C>G NCBI36
NG_008027.1:g.6611C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.65-71C>G MANE Select ENSP00000357461.3:n.65-71C>G
ENST00000636034.1:c.65-71C>G ENSP00000489703.1:n.65-71C>G
ENST00000637900.1:c.65-71C>G ENSP00000490474.1:n.65-71C>G
ENST00000368476.3:c.65-71C>G ENSP00000357461.3:n.65-71C>G
NM_000748.2:c.65-71C>G NP_000739.1:n.65-71C>G
XM_017000180.2:c.-310-71C>G XP_016855669.1:n.-310-71C>G
XR_001736952.2:n.317-71C>G
NM_000748.3:c.65-71C>G MANE Select NP_000739.1:n.65-71C>G
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