Canonical Allele Identifier: CA540074170
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1174801719
gnomAD v2: 2-234682960-C-A
gnomAD v3: 2-233774314-C-A
gnomAD v4: 2-233774314-C-A
MyVariant Identifiers: chr2:g.234682960C>A (hg19) chr2:g.233774314C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774314C>A , CM000664.2:g.233774314C>A GRCh38
NC_000002.11:g.234682960C>A , CM000664.1:g.234682960C>A GRCh37
NC_000002.10:g.234347699C>A NCBI36
NG_002601.2:g.189571C>A
NG_033238.1:g.19042C>A , LRG_733:g.19042C>A
NG_051337.1:g.3653C>A

Transcript Alleles

HGVS Amino-acid change
XM_024452842.1:c.-1458C>A XP_024308610.1:n.-1458C>A
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