Canonical Allele Identifier: CA397797920
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454406G>T , CM000679.2:g.7454406G>T GRCh38
NC_000017.10:g.7357725G>T , CM000679.1:g.7357725G>T GRCh37
NC_000017.9:g.7298449G>T NCBI36
NG_008026.1:g.14320G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.930G>T MANE Select ENSP00000304290.2:p.Lys310Asn
ENST00000306071.6:c.930G>T ENSP00000304290.2:p.Lys310Asn
ENST00000536404.6:c.714G>T ENSP00000439209.2:p.Lys238Asn
ENST00000570557.5:c.593G>T
ENST00000573209.1:n.1874G>T
ENST00000576360.1:c.605-38G>T ENSP00000459092.1:n.605-38G>T
NM_000747.2:c.930G>T NP_000738.2:p.Lys310Asn
NM_000747.3:c.930G>T MANE Select NP_000738.2:p.Lys310Asn