Canonical Allele Identifier: CA766294076
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1323215215
gnomAD v3: 2-233774371-A-C
gnomAD v4: 2-233774371-A-C
MyVariant Identifiers: chr2:g.234683017A>C (hg19) chr2:g.233774371A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774371A>C , CM000664.2:g.233774371A>C GRCh38
NC_000002.11:g.234683017A>C , CM000664.1:g.234683017A>C GRCh37
NC_000002.10:g.234347756A>C NCBI36
NG_002601.2:g.189628A>C
NG_033238.1:g.19099A>C , LRG_733:g.19099A>C
NG_051337.1:g.3710A>C

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1401A>C XP_024308610.1:n.-1401A>C
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