Canonical Allele Identifier: CA2399297381

Gene: MIAT

Linked Data

• dbSNP Id: rs1930720015

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26662785T>C , CM000684.2:g.26662785T>C	GRCh38
NC_000022.10:g.27058749T>C , CM000684.1:g.27058749T>C	GRCh37
NC_000022.9:g.25388749T>C	NCBI36
NG_016621.2:g.10304T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_003491.3:n.174-531T>C
NR_033319.2:n.174-531T>C
NR_033320.2:n.174-531T>C
NR_033321.2:n.174-531T>C