Canonical Allele Identifier: CA67601322
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs34754078
gnomAD v2: 2-234683067-C-T
gnomAD v3: 2-233774421-C-T
gnomAD v4: 2-233774421-C-T
MyVariant Identifiers: chr2:g.234683067C>T (hg19) chr2:g.233774421C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774421C>T , CM000664.2:g.233774421C>T GRCh38
NC_000002.11:g.234683067C>T , CM000664.1:g.234683067C>T GRCh37
NC_000002.10:g.234347806C>T NCBI36
NG_002601.2:g.189678C>T
NG_033238.1:g.19149C>T , LRG_733:g.19149C>T
NG_051337.1:g.3760C>T

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1351C>T XP_024308610.1:n.-1351C>T
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