Canonical Allele Identifier: CA67601309
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs745606446

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774406C>T , CM000664.2:g.233774406C>T GRCh38
NC_000002.11:g.234683052C>T , CM000664.1:g.234683052C>T GRCh37
NC_000002.10:g.234347791C>T NCBI36
NG_002601.2:g.189663C>T
NG_033238.1:g.19134C>T , LRG_733:g.19134C>T
NG_051337.1:g.3745C>T

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1366C>T XP_024308610.1:n.-1366C>T