Canonical Allele Identifier: CA67601306

Gene: MROH2A

Linked Data

• dbSNP Id: rs566338248
• gnomAD v3: 2-233774400-T-C
• gnomAD v4: 2-233774400-T-C
• MyVariant Identifiers: chr2:g.234683046T>C (hg19) ; chr2:g.233774400T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774400T>C , CM000664.2:g.233774400T>C	GRCh38
NC_000002.11:g.234683046T>C , CM000664.1:g.234683046T>C	GRCh37
NC_000002.10:g.234347785T>C	NCBI36
NG_002601.2:g.189657T>C
NG_033238.1:g.19128T>C , LRG_733:g.19128T>C
NG_051337.1:g.3739T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1372T>C	XP_024308610.1:n.-1372T>C