Canonical Allele Identifier: CA766294100

Gene: MROH2A

Linked Data

• dbSNP Id: rs1323116640
• gnomAD v3: 2-233774429-C-G
• gnomAD v4: 2-233774429-C-G
• MyVariant Identifiers: chr2:g.234683075C>G (hg19) ; chr2:g.233774429C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774429C>G , CM000664.2:g.233774429C>G	GRCh38
NC_000002.11:g.234683075C>G , CM000664.1:g.234683075C>G	GRCh37
NC_000002.10:g.234347814C>G	NCBI36
NG_002601.2:g.189686C>G
NG_033238.1:g.19157C>G , LRG_733:g.19157C>G
NG_051337.1:g.3768C>G

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1343C>G	XP_024308610.1:n.-1343C>G