Canonical Allele Identifier: CA67601327

Gene: MROH2A

Linked Data

• dbSNP Id: rs796883219
• MyVariant Identifiers: chr2:g.234683068G>A (hg19) ; chr2:g.233774422G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774422G>A , CM000664.2:g.233774422G>A	GRCh38
NC_000002.11:g.234683068G>A , CM000664.1:g.234683068G>A	GRCh37
NC_000002.10:g.234347807G>A	NCBI36
NG_002601.2:g.189679G>A
NG_033238.1:g.19150G>A , LRG_733:g.19150G>A
NG_051337.1:g.3761G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1350G>A	XP_024308610.1:n.-1350G>A