Canonical Allele Identifier: CA322664901

Gene: MIAT

Linked Data

• dbSNP Id: rs1038023196
• MyVariant Identifiers: chr22:g.27058875A>C (hg19) ; chr22:g.26662911A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26662911A>C , CM000684.2:g.26662911A>C	GRCh38
NC_000022.10:g.27058875A>C , CM000684.1:g.27058875A>C	GRCh37
NC_000022.9:g.25388875A>C	NCBI36
NG_016621.2:g.10430A>C

Transcript Alleles

HGVS	Amino-acid change
NR_003491.3:n.174-405A>C
NR_033319.2:n.174-405A>C
NR_033320.2:n.174-405A>C
NR_033321.2:n.174-405A>C