Canonical Allele Identifier: CA540074302
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1197690810

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774523A>G , CM000664.2:g.233774523A>G GRCh38
NC_000002.11:g.234683169A>G , CM000664.1:g.234683169A>G GRCh37
NC_000002.10:g.234347908A>G NCBI36
NG_002601.2:g.189780A>G
NG_033238.1:g.19251A>G , LRG_733:g.19251A>G
NG_051337.1:g.3862A>G

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1249A>G XP_024308610.1:n.-1249A>G