Canonical Allele Identifier: CA497740302
Gene: CHRNB1 HGNC NCBI

Linked Data

gnomAD v4: 17-7445143-C-T
MyVariant Identifiers: chr17:g.7348462C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445143C>T , CM000679.2:g.7445143C>T GRCh38
NC_000017.10:g.7348462C>T , CM000679.1:g.7348462C>T GRCh37
NC_000017.9:g.7289186C>T NCBI36
NG_008026.1:g.5057C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.16C>T MANE Select ENSP00000304290.2:p.Leu6=
ENST00000306071.6:c.16C>T ENSP00000304290.2:p.Leu6=
ENST00000572857.5:c.16C>T ENSP00000461402.1:p.Leu6=
ENST00000574054.1:n.36C>T
NM_000747.2:c.16C>T NP_000738.2:p.Leu6=
NM_000747.3:c.16C>T MANE Select NP_000738.2:p.Leu6=