Canonical Allele Identifier: CA938709460
Gene: CHRM1 HGNC NCBI

Linked Data

dbSNP Id: rs2085854271
gnomAD v3: 11-62909362-C-T
gnomAD v4: 11-62909362-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62909362C>T , CM000673.2:g.62909362C>T GRCh38
NC_000011.9:g.62676834C>T , CM000673.1:g.62676834C>T GRCh37
NC_000011.8:g.62433410C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306960.4:c.*356G>A MANE Select ENSP00000306490.3:n.*356G>A
ENST00000306960.3:c.*356G>A ENSP00000306490.3:n.*356G>A
NM_000738.2:c.*356G>A NP_000729.2:n.*356G>A
XM_011544742.1:c.*356G>A XP_011543044.1:n.*356G>A
XM_011544742.2:c.*356G>A XP_011543044.1:n.*356G>A
NM_000738.3:c.*356G>A MANE Select NP_000729.2:n.*356G>A
Search 100 bp 5'
Search 100 bp 3'