Canonical Allele Identifier: CA223645223
Gene: CHRM1 HGNC NCBI

Linked Data

dbSNP Id: rs1031880224
gnomAD v2: 11-62676835-T-G
gnomAD v3: 11-62909363-T-G
gnomAD v4: 11-62909363-T-G
MyVariant Identifiers: chr11:g.62676835T>G (hg19) chr11:g.62909363T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62909363T>G , CM000673.2:g.62909363T>G GRCh38
NC_000011.9:g.62676835T>G , CM000673.1:g.62676835T>G GRCh37
NC_000011.8:g.62433411T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306960.4:c.*355A>C MANE Select ENSP00000306490.3:n.*355A>C
ENST00000306960.3:c.*355A>C ENSP00000306490.3:n.*355A>C
NM_000738.2:c.*355A>C NP_000729.2:n.*355A>C
XM_011544742.1:c.*355A>C XP_011543044.1:n.*355A>C
XM_011544742.2:c.*355A>C XP_011543044.1:n.*355A>C
NM_000738.3:c.*355A>C MANE Select NP_000729.2:n.*355A>C
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