Canonical Allele Identifier: CA638869677
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1459641928
gnomAD v2: 22-27058676-C-G
MyVariant Identifiers: chr22:g.27058676C>G (hg19) chr22:g.26662712C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662712C>G , CM000684.2:g.26662712C>G GRCh38
NC_000022.10:g.27058676C>G , CM000684.1:g.27058676C>G GRCh37
NC_000022.9:g.25388676C>G NCBI36
NG_016621.2:g.10231C>G

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-604C>G
NR_033319.2:n.174-604C>G
NR_033320.2:n.174-604C>G
NR_033321.2:n.174-604C>G
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