Canonical Allele Identifier: CA679097236
Gene: CHRM1 HGNC NCBI

Linked Data

dbSNP Id: rs1371994311
gnomAD v3: 11-62909247-TC-T
gnomAD v4: 11-62909247-TC-T
MyVariant Identifiers: chr11:g.62676720del (hg19) chr11:g.62909248del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62909251del , CM000673.2:g.62909251del GRCh38
NC_000011.9:g.62676723del , CM000673.1:g.62676723del GRCh37
NC_000011.8:g.62433299del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306960.4:c.*470del MANE Select ENSP00000306490.3:n.*470del
ENST00000306960.3:c.*470del ENSP00000306490.3:n.*470del
NM_000738.2:c.*470del NP_000729.2:n.*470del
XM_011544742.1:c.*470del XP_011543044.1:n.*470del
XM_011544742.2:c.*470del XP_011543044.1:n.*470del
NM_000738.3:c.*470del MANE Select NP_000729.2:n.*470del
Search 100 bp 5'
Search 100 bp 3'