Canonical Allele Identifier: CA766294112
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1189089545

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774480A>T , CM000664.2:g.233774480A>T GRCh38
NC_000002.11:g.234683126A>T , CM000664.1:g.234683126A>T GRCh37
NC_000002.10:g.234347865A>T NCBI36
NG_002601.2:g.189737A>T
NG_033238.1:g.19208A>T , LRG_733:g.19208A>T
NG_051337.1:g.3819A>T

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1292A>T XP_024308610.1:n.-1292A>T