Canonical Allele Identifier: CA67604338

Gene: MROH2A

Linked Data

• dbSNP Id: rs939132888
• MyVariant Identifiers: chr2:g.234687339G>A (hg19) ; chr2:g.233778693G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233778693G>A , CM000664.2:g.233778693G>A	GRCh38
NC_000002.11:g.234687339G>A , CM000664.1:g.234687339G>A	GRCh37
NC_000002.10:g.234352078G>A	NCBI36
NG_051337.1:g.8032G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000389758.4:c.-15+212G>A MANE Select	ENSP00000374408.3:n.-15+212G>A
ENST00000389758.3:c.-15+212G>A	ENSP00000374408.3:n.-15+212G>A
ENST00000428446.5:c.-12-654G>A	ENSP00000404614.1:n.-12-654G>A
ENST00000430892.5:c.-14-652G>A	ENSP00000392128.1:n.-14-652G>A
ENST00000454283.1:c.-83-978G>A	ENSP00000409355.1:n.-83-978G>A
ENST00000610772.4:c.-14-652G>A	ENSP00000477597.1:n.-14-652G>A
NM_001287395.1:c.-14-652G>A	NP_001274324.1:n.-14-652G>A
XM_011511075.1:c.76+212G>A	XP_011509377.1:n.76+212G>A
XM_011511076.1:c.76+212G>A	XP_011509378.1:n.76+212G>A
XM_011511077.1:c.76+212G>A	XP_011509379.1:n.76+212G>A
XM_011511078.1:c.76+212G>A	XP_011509380.1:n.76+212G>A
XM_011511079.1:c.76+212G>A	XP_011509381.1:n.76+212G>A
XM_011511080.1:c.-14-652G>A	XP_011509382.1:n.-14-652G>A
XM_011511081.1:c.76+212G>A	XP_011509383.1:n.76+212G>A
XM_011511082.1:c.76+212G>A	XP_011509384.1:n.76+212G>A
XM_011511083.1:c.76+212G>A	XP_011509385.1:n.76+212G>A
XM_011511084.1:c.76+212G>A	XP_011509386.1:n.76+212G>A
XM_011511086.1:c.76+212G>A	XP_011509388.1:n.76+212G>A
XM_011511076.2:c.76+212G>A	XP_011509378.1:n.76+212G>A
XM_011511086.2:c.76+212G>A	XP_011509388.1:n.76+212G>A
XM_024452839.1:c.76+212G>A	XP_024308607.1:n.76+212G>A
XM_024452840.1:c.76+212G>A	XP_024308608.1:n.76+212G>A
XM_024452841.1:c.76+212G>A	XP_024308609.1:n.76+212G>A
XM_024452842.1:c.-14-652G>A	XP_024308610.1:n.-14-652G>A
XM_024452843.1:c.76+212G>A	XP_024308611.1:n.76+212G>A
XM_024452844.1:c.76+212G>A	XP_024308612.1:n.76+212G>A
XM_024452845.1:c.76+212G>A	XP_024308613.1:n.76+212G>A
XM_024452846.1:c.76+212G>A	XP_024308614.1:n.76+212G>A
NM_001367507.1:c.-14-652G>A	NP_001354436.1:n.-14-652G>A
NM_001394639.1:c.-15+212G>A MANE Select	NP_001381568.1:n.-15+212G>A