Canonical Allele Identifier: CA1043573591
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1700633457

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774397T>C , CM000664.2:g.233774397T>C GRCh38
NC_000002.11:g.234683043T>C , CM000664.1:g.234683043T>C GRCh37
NC_000002.10:g.234347782T>C NCBI36
NG_002601.2:g.189654T>C
NG_033238.1:g.19125T>C , LRG_733:g.19125T>C
NG_051337.1:g.3736T>C

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1375T>C XP_024308610.1:n.-1375T>C