Canonical Allele Identifier: CA2399297421
Gene: MIAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662904_26662905delinsAG , CM000684.2:g.26662904_26662905delinsAG GRCh38
NC_000022.10:g.27058868_27058869delinsAG , CM000684.1:g.27058868_27058869delinsAG GRCh37
NC_000022.9:g.25388868_25388869delinsAG NCBI36
NG_016621.2:g.10423_10424delinsAG

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-412_174-411delinsAG
NR_033319.2:n.174-412_174-411delinsAG
NR_033320.2:n.174-412_174-411delinsAG
NR_033321.2:n.174-412_174-411delinsAG