Canonical Allele Identifier: CA766294070

Gene: MROH2A

Linked Data

• dbSNP Id: rs1397456033
• gnomAD v3: 2-233774349-A-G
• gnomAD v4: 2-233774349-A-G
• MyVariant Identifiers: chr2:g.234682995A>G (hg19) ; chr2:g.233774349A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774349A>G , CM000664.2:g.233774349A>G	GRCh38
NC_000002.11:g.234682995A>G , CM000664.1:g.234682995A>G	GRCh37
NC_000002.10:g.234347734A>G	NCBI36
NG_002601.2:g.189606A>G
NG_033238.1:g.19077A>G , LRG_733:g.19077A>G
NG_051337.1:g.3688A>G

Transcript Alleles

HGVS	Amino-acid change
XM_024452842.1:c.-1423A>G	XP_024308610.1:n.-1423A>G