Canonical Allele Identifier: CA223645198
Gene: CHRM1 HGNC NCBI

Linked Data

dbSNP Id: rs552102877

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62909348T>C , CM000673.2:g.62909348T>C GRCh38
NC_000011.9:g.62676820T>C , CM000673.1:g.62676820T>C GRCh37
NC_000011.8:g.62433396T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306960.4:c.*370A>G MANE Select ENSP00000306490.3:n.*370A>G
ENST00000306960.3:c.*370A>G ENSP00000306490.3:n.*370A>G
NM_000738.2:c.*370A>G NP_000729.2:n.*370A>G
XM_011544742.1:c.*370A>G XP_011543044.1:n.*370A>G
XM_011544742.2:c.*370A>G XP_011543044.1:n.*370A>G
NM_000738.3:c.*370A>G MANE Select NP_000729.2:n.*370A>G