Canonical Allele Identifier: CA2556930055
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455771G>T , CM000679.2:g.7455771G>T GRCh38
NC_000017.10:g.7359090G>T , CM000679.1:g.7359090G>T GRCh37
NC_000017.9:g.7299814G>T NCBI36
NG_008026.1:g.15685G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1218-23G>T MANE Select ENSP00000304290.2:n.1218-23G>T
ENST00000306071.6:c.1218-23G>T ENSP00000304290.2:n.1218-23G>T
ENST00000536404.6:c.1002-23G>T ENSP00000439209.2:n.1002-23G>T
ENST00000570557.5:c.881-23G>T
ENST00000575379.1:c.-198G>T ENSP00000461751.1:n.-198G>T
ENST00000576360.1:c.855-23G>T ENSP00000459092.1:n.855-23G>T
NM_000747.2:c.1218-23G>T NP_000738.2:n.1218-23G>T
NM_000747.3:c.1218-23G>T MANE Select NP_000738.2:n.1218-23G>T