Canonical Allele Identifier: CA540074279
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1330735629

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774467A>C , CM000664.2:g.233774467A>C GRCh38
NC_000002.11:g.234683113A>C , CM000664.1:g.234683113A>C GRCh37
NC_000002.10:g.234347852A>C NCBI36
NG_002601.2:g.189724A>C
NG_033238.1:g.19195A>C , LRG_733:g.19195A>C
NG_051337.1:g.3806A>C

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1305A>C XP_024308610.1:n.-1305A>C