Canonical Allele Identifier: CA1672894406
Gene: ARMT1 HGNC NCBI

Linked Data

dbSNP Id: rs963193
gnomAD v4: 6-151468220-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468220T>A , CM000668.2:g.151468220T>A GRCh38
NC_000006.11:g.151789355T>A , CM000668.1:g.151789355T>A GRCh37
NC_000006.10:g.151831048T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000367294.4:c.559-123T>A MANE Select ENSP00000356263.3:n.559-123T>A
ENST00000367294.3:c.559-123T>A ENSP00000356263.3:n.559-123T>A
ENST00000494826.1:c.*282-123T>A ENSP00000435882.1:n.*282-123T>A
ENST00000545879.5:c.202-123T>A ENSP00000444121.1:n.202-123T>A
NM_001286562.1:c.202-123T>A NP_001273491.1:n.202-123T>A
NM_024573.2:c.559-123T>A NP_078849.1:n.559-123T>A
NM_024573.3:c.559-123T>A MANE Select NP_078849.1:n.559-123T>A
NM_001286562.2:c.202-123T>A NP_001273491.1:n.202-123T>A
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