Canonical Allele Identifier: CA1335897924
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1500482

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774392C>G , CM000664.2:g.233774392C>G GRCh38
NC_000002.11:g.234683038C>G , CM000664.1:g.234683038C>G GRCh37
NC_000002.10:g.234347777C>G NCBI36
NG_002601.2:g.189649C>G
NG_033238.1:g.19120C>G , LRG_733:g.19120C>G
NG_051337.1:g.3731C>G

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1380C>G XP_024308610.1:n.-1380C>G