Canonical Allele Identifier: CA752042675

Gene: MIAT

Linked Data

• dbSNP Id: rs1396988762
• MyVariant Identifiers: chr22:g.27058789A>C (hg19) ; chr22:g.26662825A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26662825A>C , CM000684.2:g.26662825A>C	GRCh38
NC_000022.10:g.27058789A>C , CM000684.1:g.27058789A>C	GRCh37
NC_000022.9:g.25388789A>C	NCBI36
NG_016621.2:g.10344A>C

Transcript Alleles

HGVS	Amino-acid change
NR_003491.3:n.174-491A>C
NR_033319.2:n.174-491A>C
NR_033320.2:n.174-491A>C
NR_033321.2:n.174-491A>C