Canonical Allele Identifier: CA2635846319
Gene: CHRNB1 HGNC NCBI

Linked Data

gnomAD v4: 17-7454603-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454603G>T , CM000679.2:g.7454603G>T GRCh38
NC_000017.10:g.7357922G>T , CM000679.1:g.7357922G>T GRCh37
NC_000017.9:g.7298646G>T NCBI36
NG_008026.1:g.14517G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1044+83G>T MANE Select ENSP00000304290.2:n.1044+83G>T
ENST00000306071.6:c.1044+83G>T ENSP00000304290.2:n.1044+83G>T
ENST00000536404.6:c.828+83G>T ENSP00000439209.2:n.828+83G>T
ENST00000570557.5:c.707+83G>T
ENST00000573209.1:n.1988+83G>T
ENST00000576360.1:c.681+83G>T ENSP00000459092.1:n.681+83G>T
NM_000747.2:c.1044+83G>T NP_000738.2:n.1044+83G>T
NM_000747.3:c.1044+83G>T MANE Select NP_000738.2:n.1044+83G>T
Search 100 bp 5'
Search 100 bp 3'