Canonical Allele Identifier: CA1977998397
Gene: CHRM1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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