Canonical Allele Identifier: CA2687122798
Gene: CHRNB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42732639_42732640insACAATA , CM000670.2:g.42732639_42732640insACAATA GRCh38
NC_000008.10:g.42587782_42587783insACAATA , CM000670.1:g.42587782_42587783insACAATA GRCh37
NC_000008.9:g.42706939_42706940insACAATA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289957.3:c.1242+90_1242+91insACAATA MANE Select ENSP00000289957.2:n.1242+90_1242+91insACAATA
ENST00000289957.2:c.1242+90_1242+91insACAATA ENSP00000289957.2:n.1242+90_1242+91insACAATA
NM_000749.3:c.1242+90_1242+91insACAATA NP_000740.1:n.1242+90_1242+91insACAATA
XM_011544390.1:c.855+90_855+91insACAATA XP_011542692.1:n.855+90_855+91insACAATA
NM_000749.4:c.1242+90_1242+91insACAATA NP_000740.1:n.1242+90_1242+91insACAATA
NM_001347717.1:c.1020+90_1020+91insACAATA NP_001334646.1:n.1020+90_1020+91insACAATA
XM_011544390.2:c.855+90_855+91insACAATA XP_011542692.1:n.855+90_855+91insACAATA
NM_000749.5:c.1242+90_1242+91insACAATA MANE Select NP_000740.1:n.1242+90_1242+91insACAATA
NM_001347717.2:c.1020+90_1020+91insACAATA NP_001334646.1:n.1020+90_1020+91insACAATA