Canonical Allele Identifier: CA17964022
Gene: MTOR HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.11262852G>T
GRCh37 chr1:g.11322909G>T
gnomAD v2:
1:11322909 G / T
gnomAD v3:
1:11262852 G / T
gnomAD v4:
chr1-11262852-G-T
Joint Max Group AF 0.07039292 (AFR)
Genomes Max Group AF 0.07039292 (AFR)
ClinVar RCV:
RCV001516414
ClinVar Variation:
1167316
dbSNP:
17027478
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11262852G>T , CM000663.2:g.11262852G>T GRCh38
NC_000001.10:g.11322909G>T , CM000663.1:g.11322909G>T GRCh37
NC_000001.9:g.11245496G>T NCBI36
NG_033239.1:g.4700C>A , LRG_734:g.4700C>A

Transcript Alleles

HGVS Amino-acid Change
XM_024446187.1:c.-422C>A XP_024301955.1:n.-422C>A
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