Canonical Allele Identifier: CA497740609
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7348531G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445212G>T , CM000679.2:g.7445212G>T GRCh38
NC_000017.10:g.7348531G>T , CM000679.1:g.7348531G>T GRCh37
NC_000017.9:g.7289255G>T NCBI36
NG_008026.1:g.5126G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.58+27G>T MANE Select ENSP00000304290.2:n.58+27G>T
ENST00000306071.6:c.58+27G>T ENSP00000304290.2:n.58+27G>T
ENST00000572857.5:c.58+27G>T ENSP00000461402.1:n.58+27G>T
ENST00000574054.1:n.78+27G>T
NM_000747.2:c.58+27G>T NP_000738.2:n.58+27G>T
NM_000747.3:c.58+27G>T MANE Select NP_000738.2:n.58+27G>T
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