Canonical Allele Identifier: CA1043573560
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1202918379
gnomAD v3: 2-233774303-C-T
gnomAD v4: 2-233774303-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774303C>T , CM000664.2:g.233774303C>T GRCh38
NC_000002.11:g.234682949C>T , CM000664.1:g.234682949C>T GRCh37
NC_000002.10:g.234347688C>T NCBI36
NG_002601.2:g.189560C>T
NG_033238.1:g.19031C>T , LRG_733:g.19031C>T
NG_051337.1:g.3642C>T

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1469C>T XP_024308610.1:n.-1469C>T
Search 100 bp 5'
Search 100 bp 3'