Canonical Allele Identifier: CA1043573551

Gene: MROH2A

Linked Data

• dbSNP Id: rs1700628143
• gnomAD v3: 2-233774289-CTCT-C
• gnomAD v4: 2-233774289-CTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774291_233774293del , CM000664.2:g.233774291_233774293del	GRCh38
NC_000002.11:g.234682937_234682939del , CM000664.1:g.234682937_234682939del	GRCh37
NC_000002.10:g.234347676_234347678del	NCBI36
NG_002601.2:g.189548_189550del
NG_033238.1:g.19019_19021del , LRG_733:g.19019_19021del
NG_051337.1:g.3630_3632del

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1481_-1479del	XP_024308610.1:n.-1481_-1479del