Canonical Allele Identifier: CA397798561
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454473C>G , CM000679.2:g.7454473C>G GRCh38
NC_000017.10:g.7357792C>G , CM000679.1:g.7357792C>G GRCh37
NC_000017.9:g.7298516C>G NCBI36
NG_008026.1:g.14387C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.997C>G MANE Select ENSP00000304290.2:p.His333Asp
ENST00000306071.6:c.997C>G ENSP00000304290.2:p.His333Asp
ENST00000536404.6:c.781C>G ENSP00000439209.2:p.His261Asp
ENST00000570557.5:c.660C>G
ENST00000573209.1:n.1941C>G
ENST00000576360.1:c.634C>G ENSP00000459092.1:p.His212Asp
NM_000747.2:c.997C>G NP_000738.2:p.His333Asp
NM_000747.3:c.997C>G MANE Select NP_000738.2:p.His333Asp