Canonical Allele Identifier: CA766294055
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1484265869
gnomAD v3: 2-233774294-G-A
gnomAD v4: 2-233774294-G-A
MyVariant Identifiers: chr2:g.234682940G>A (hg19) chr2:g.233774294G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774294G>A , CM000664.2:g.233774294G>A GRCh38
NC_000002.11:g.234682940G>A , CM000664.1:g.234682940G>A GRCh37
NC_000002.10:g.234347679G>A NCBI36
NG_002601.2:g.189551G>A
NG_033238.1:g.19022G>A , LRG_733:g.19022G>A
NG_051337.1:g.3633G>A

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1478G>A XP_024308610.1:n.-1478G>A
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