Canonical Allele Identifier: CA752042611
Gene: MIAT HGNC NCBI

Linked Data

dbSNP Id: rs1434578842
MyVariant Identifiers: chr22:g.27058628C>T (hg19) chr22:g.26662664C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662664C>T , CM000684.2:g.26662664C>T GRCh38
NC_000022.10:g.27058628C>T , CM000684.1:g.27058628C>T GRCh37
NC_000022.9:g.25388628C>T NCBI36
NG_016621.2:g.10183C>T

Transcript Alleles

HGVS Amino-acid change
NR_003491.3:n.174-652C>T
NR_033319.2:n.174-652C>T
NR_033320.2:n.174-652C>T
NR_033321.2:n.174-652C>T
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