Canonical Allele Identifier: CA397786163
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445138G>T , CM000679.2:g.7445138G>T GRCh38
NC_000017.10:g.7348457G>T , CM000679.1:g.7348457G>T GRCh37
NC_000017.9:g.7289181G>T NCBI36
NG_008026.1:g.5052G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.11G>T MANE Select ENSP00000304290.2:p.Gly4Val
ENST00000306071.6:c.11G>T ENSP00000304290.2:p.Gly4Val
ENST00000572857.5:c.11G>T ENSP00000461402.1:p.Gly4Val
ENST00000574054.1:n.31G>T
NM_000747.2:c.11G>T NP_000738.2:p.Gly4Val
NM_000747.3:c.11G>T MANE Select NP_000738.2:p.Gly4Val