Canonical Allele Identifier: CA2614024662
Gene: CHRM1 HGNC NCBI

Linked Data

gnomAD v4: 11-62909379-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.62909379T>C , CM000673.2:g.62909379T>C GRCh38
NC_000011.9:g.62676851T>C , CM000673.1:g.62676851T>C GRCh37
NC_000011.8:g.62433427T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306960.4:c.*339A>G MANE Select ENSP00000306490.3:n.*339A>G
ENST00000306960.3:c.*339A>G ENSP00000306490.3:n.*339A>G
NM_000738.2:c.*339A>G NP_000729.2:n.*339A>G
XM_011544742.1:c.*339A>G XP_011543044.1:n.*339A>G
XM_011544742.2:c.*339A>G XP_011543044.1:n.*339A>G
NM_000738.3:c.*339A>G MANE Select NP_000729.2:n.*339A>G
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