Canonical Allele Identifier: CA150146712
Gene: ARMT1 HGNC NCBI

Linked Data

dbSNP Id: rs867887838
MyVariant Identifiers: chr6:g.151789302G>T (hg19) chr6:g.151468167G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468167G>T , CM000668.2:g.151468167G>T GRCh38
NC_000006.11:g.151789302G>T , CM000668.1:g.151789302G>T GRCh37
NC_000006.10:g.151830995G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-176G>T MANE Select ENSP00000356263.3:n.559-176G>T
ENST00000367294.3:c.559-176G>T ENSP00000356263.3:n.559-176G>T
ENST00000494826.1:c.*282-176G>T ENSP00000435882.1:n.*282-176G>T
ENST00000545879.5:c.202-176G>T ENSP00000444121.1:n.202-176G>T
NM_001286562.1:c.202-176G>T NP_001273491.1:n.202-176G>T
NM_024573.2:c.559-176G>T NP_078849.1:n.559-176G>T
NM_024573.3:c.559-176G>T MANE Select NP_078849.1:n.559-176G>T
NM_001286562.2:c.202-176G>T NP_001273491.1:n.202-176G>T
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