Canonical Allele Identifier: CA397786136
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445135C>G , CM000679.2:g.7445135C>G GRCh38
NC_000017.10:g.7348454C>G , CM000679.1:g.7348454C>G GRCh37
NC_000017.9:g.7289178C>G NCBI36
NG_008026.1:g.5049C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.8C>G MANE Select ENSP00000304290.2:p.Pro3Arg
ENST00000306071.6:c.8C>G ENSP00000304290.2:p.Pro3Arg
ENST00000572857.5:c.8C>G ENSP00000461402.1:p.Pro3Arg
ENST00000574054.1:n.28C>G
NM_000747.2:c.8C>G NP_000738.2:p.Pro3Arg
NM_000747.3:c.8C>G MANE Select NP_000738.2:p.Pro3Arg