Canonical Allele Identifier: CA497740611
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1326078891
gnomAD v4: 17-7445213-A-G
MyVariant Identifiers: chr17:g.7348532A>G (hg19) chr17:g.7445213A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445213A>G , CM000679.2:g.7445213A>G GRCh38
NC_000017.10:g.7348532A>G , CM000679.1:g.7348532A>G GRCh37
NC_000017.9:g.7289256A>G NCBI36
NG_008026.1:g.5127A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.58+28A>G MANE Select ENSP00000304290.2:n.58+28A>G
ENST00000306071.6:c.58+28A>G ENSP00000304290.2:n.58+28A>G
ENST00000572857.5:c.58+28A>G ENSP00000461402.1:n.58+28A>G
ENST00000574054.1:n.78+28A>G
NM_000747.2:c.58+28A>G NP_000738.2:n.58+28A>G
NM_000747.3:c.58+28A>G MANE Select NP_000738.2:n.58+28A>G
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