Canonical Allele Identifier: CA1779564464
Gene: CHRNB3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42732817T= , CM000670.2:g.42732817T= GRCh38
NC_000008.10:g.42587960T= , CM000670.1:g.42587960T= GRCh37
NC_000008.9:g.42707117T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289957.3:c.1242+268T= MANE Select ENSP00000289957.2:n.1242+268T=
ENST00000289957.2:c.1242+268T= ENSP00000289957.2:n.1242+268T=
NM_000749.3:c.1242+268T= NP_000740.1:n.1242+268T=
XM_011544390.1:c.855+268T= XP_011542692.1:n.855+268T=
NM_000749.4:c.1242+268T= NP_000740.1:n.1242+268T=
NM_001347717.1:c.1020+268T= NP_001334646.1:n.1020+268T=
XM_011544390.2:c.855+268T= XP_011542692.1:n.855+268T=
NM_000749.5:c.1242+268T= MANE Select NP_000740.1:n.1242+268T=
NM_001347717.2:c.1020+268T= NP_001334646.1:n.1020+268T=
Search 100 bp 5'
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