Canonical Allele Identifier: CA2576152149
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454200C>T , CM000679.2:g.7454200C>T GRCh38
NC_000017.10:g.7357519C>T , CM000679.1:g.7357519C>T GRCh37
NC_000017.9:g.7298243C>T NCBI36
NG_008026.1:g.14114C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-97C>T MANE Select ENSP00000304290.2:n.821-97C>T
ENST00000306071.6:c.821-97C>T ENSP00000304290.2:n.821-97C>T
ENST00000536404.6:c.605-97C>T ENSP00000439209.2:n.605-97C>T
ENST00000570557.5:c.484-97C>T
ENST00000573209.1:n.1765-97C>T
ENST00000576360.1:c.605-244C>T ENSP00000459092.1:n.605-244C>T
NM_000747.2:c.821-97C>T NP_000738.2:n.821-97C>T
NM_000747.3:c.821-97C>T MANE Select NP_000738.2:n.821-97C>T