Canonical Allele Identifier: CA322664911
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs764583634
gnomAD v3: 22-26663025-G-C
gnomAD v4: 22-26663025-G-C
MyVariant Identifiers: chr22:g.27058989G>C (hg19) chr22:g.26663025G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26663025G>C , CM000684.2:g.26663025G>C GRCh38
NC_000022.10:g.27058989G>C , CM000684.1:g.27058989G>C GRCh37
NC_000022.9:g.25388989G>C NCBI36
NG_016621.2:g.10544G>C

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-291G>C
NR_033319.2:n.174-291G>C
NR_033320.2:n.174-291G>C
NR_033321.2:n.174-291G>C
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