Canonical Allele Identifier: CA223645212
Gene: CHRM1 HGNC NCBI

Linked Data

dbSNP Id: rs565560808
gnomAD v3: 11-62909359-A-G
gnomAD v4: 11-62909359-A-G
MyVariant Identifiers: chr11:g.62676831A>G (hg19) chr11:g.62909359A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62909359A>G , CM000673.2:g.62909359A>G GRCh38
NC_000011.9:g.62676831A>G , CM000673.1:g.62676831A>G GRCh37
NC_000011.8:g.62433407A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306960.4:c.*359T>C MANE Select ENSP00000306490.3:n.*359T>C
ENST00000306960.3:c.*359T>C ENSP00000306490.3:n.*359T>C
NM_000738.2:c.*359T>C NP_000729.2:n.*359T>C
XM_011544742.1:c.*359T>C XP_011543044.1:n.*359T>C
XM_011544742.2:c.*359T>C XP_011543044.1:n.*359T>C
NM_000738.3:c.*359T>C MANE Select NP_000729.2:n.*359T>C
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