Canonical Allele Identifier: CA1024749562
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1664840920
gnomAD v3: 22-26662974-A-G
gnomAD v4: 22-26662974-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662974A>G , CM000684.2:g.26662974A>G GRCh38
NC_000022.10:g.27058938A>G , CM000684.1:g.27058938A>G GRCh37
NC_000022.9:g.25388938A>G NCBI36
NG_016621.2:g.10493A>G

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-342A>G
NR_033319.2:n.174-342A>G
NR_033320.2:n.174-342A>G
NR_033321.2:n.174-342A>G
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