Canonical Allele Identifier: CA67601333

Gene: MROH2A

Linked Data

• dbSNP Id: rs940687513
• gnomAD v3: 2-233774485-G-A
• gnomAD v4: 2-233774485-G-A
• MyVariant Identifiers: chr2:g.234683131G>A (hg19) ; chr2:g.233774485G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774485G>A , CM000664.2:g.233774485G>A	GRCh38
NC_000002.11:g.234683131G>A , CM000664.1:g.234683131G>A	GRCh37
NC_000002.10:g.234347870G>A	NCBI36
NG_002601.2:g.189742G>A
NG_033238.1:g.19213G>A , LRG_733:g.19213G>A
NG_051337.1:g.3824G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1287G>A	XP_024308610.1:n.-1287G>A