Canonical Allele Identifier: CA2701877631
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs2126069920

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774419A>G , CM000664.2:g.233774419A>G GRCh38
NC_000002.11:g.234683065A>G , CM000664.1:g.234683065A>G GRCh37
NC_000002.10:g.234347804A>G NCBI36
NG_002601.2:g.189676A>G
NG_033238.1:g.19147A>G , LRG_733:g.19147A>G
NG_051337.1:g.3758A>G

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1353A>G XP_024308610.1:n.-1353A>G