Canonical Allele Identifier: CA397786130
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445134C>T , CM000679.2:g.7445134C>T GRCh38
NC_000017.10:g.7348453C>T , CM000679.1:g.7348453C>T GRCh37
NC_000017.9:g.7289177C>T NCBI36
NG_008026.1:g.5048C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.7C>T MANE Select ENSP00000304290.2:p.Pro3Ser
ENST00000306071.6:c.7C>T ENSP00000304290.2:p.Pro3Ser
ENST00000572857.5:c.7C>T ENSP00000461402.1:p.Pro3Ser
ENST00000574054.1:n.27C>T
NM_000747.2:c.7C>T NP_000738.2:p.Pro3Ser
NM_000747.3:c.7C>T MANE Select NP_000738.2:p.Pro3Ser