Canonical Allele Identifier: CA1335897928
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1700633376

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774396G>C , CM000664.2:g.233774396G>C GRCh38
NC_000002.11:g.234683042G>C , CM000664.1:g.234683042G>C GRCh37
NC_000002.10:g.234347781G>C NCBI36
NG_002601.2:g.189653G>C
NG_033238.1:g.19124G>C , LRG_733:g.19124G>C
NG_051337.1:g.3735G>C

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1376G>C XP_024308610.1:n.-1376G>C