Canonical Allele Identifier: CA67601331

Gene: MROH2A

Linked Data

• dbSNP Id: rs558537844
• gnomAD v3: 2-233774432-G-C
• MyVariant Identifiers: chr2:g.234683078G>C (hg19) ; chr2:g.233774432G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774432G>C , CM000664.2:g.233774432G>C	GRCh38
NC_000002.11:g.234683078G>C , CM000664.1:g.234683078G>C	GRCh37
NC_000002.10:g.234347817G>C	NCBI36
NG_002601.2:g.189689G>C
NG_033238.1:g.19160G>C , LRG_733:g.19160G>C
NG_051337.1:g.3771G>C

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1340G>C	XP_024308610.1:n.-1340G>C