Canonical Allele Identifier: CA2576152184
Gene: CHRNB1 HGNC NCBI

Linked Data

gnomAD v4: 17-7454223-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454223A>G , CM000679.2:g.7454223A>G GRCh38
NC_000017.10:g.7357542A>G , CM000679.1:g.7357542A>G GRCh37
NC_000017.9:g.7298266A>G NCBI36
NG_008026.1:g.14137A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-74A>G MANE Select ENSP00000304290.2:n.821-74A>G
ENST00000306071.6:c.821-74A>G ENSP00000304290.2:n.821-74A>G
ENST00000536404.6:c.605-74A>G ENSP00000439209.2:n.605-74A>G
ENST00000570557.5:c.484-74A>G
ENST00000573209.1:n.1765-74A>G
ENST00000576360.1:c.605-221A>G ENSP00000459092.1:n.605-221A>G
NM_000747.2:c.821-74A>G NP_000738.2:n.821-74A>G
NM_000747.3:c.821-74A>G MANE Select NP_000738.2:n.821-74A>G