Canonical Allele Identifier: CA540074171
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1391084100
gnomAD v2: 2-234682972-C-T
gnomAD v3: 2-233774326-C-T
gnomAD v4: 2-233774326-C-T
MyVariant Identifiers: chr2:g.234682972C>T (hg19) chr2:g.233774326C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774326C>T , CM000664.2:g.233774326C>T GRCh38
NC_000002.11:g.234682972C>T , CM000664.1:g.234682972C>T GRCh37
NC_000002.10:g.234347711C>T NCBI36
NG_002601.2:g.189583C>T
NG_033238.1:g.19054C>T , LRG_733:g.19054C>T
NG_051337.1:g.3665C>T

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1446C>T XP_024308610.1:n.-1446C>T
Search 100 bp 5'
Search 100 bp 3'