Canonical Allele Identifier: CA599571233
Gene: CHRM1 HGNC NCBI

Linked Data

dbSNP Id: rs1270381574
gnomAD v2: 11-62676850-C-G
gnomAD v4: 11-62909378-C-G
MyVariant Identifiers: chr11:g.62676850C>G (hg19) chr11:g.62909378C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62909378C>G , CM000673.2:g.62909378C>G GRCh38
NC_000011.9:g.62676850C>G , CM000673.1:g.62676850C>G GRCh37
NC_000011.8:g.62433426C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306960.4:c.*340G>C MANE Select ENSP00000306490.3:n.*340G>C
ENST00000306960.3:c.*340G>C ENSP00000306490.3:n.*340G>C
NM_000738.2:c.*340G>C NP_000729.2:n.*340G>C
XM_011544742.1:c.*340G>C XP_011543044.1:n.*340G>C
XM_011544742.2:c.*340G>C XP_011543044.1:n.*340G>C
NM_000738.3:c.*340G>C MANE Select NP_000729.2:n.*340G>C
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