Canonical Allele Identifier: CA2245842139
Gene: CHRNB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445130G= , CM000679.2:g.7445130G= GRCh38
NC_000017.10:g.7348449G= , CM000679.1:g.7348449G= GRCh37
NC_000017.9:g.7289173G= NCBI36
NG_008026.1:g.5044G=

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.3G= MANE Select ENSP00000304290.2:p.Met1=
ENST00000306071.6:c.3G= ENSP00000304290.2:p.Met1=
ENST00000572857.5:c.3G= ENSP00000461402.1:p.Met1=
ENST00000574054.1:n.23G=
NM_000747.2:c.3G= NP_000738.2:p.Met1=
NM_000747.3:c.3G= MANE Select NP_000738.2:p.Met1=