Canonical Allele Identifier: CA1335897902
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1379211912
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774351A>G , CM000664.2:g.233774351A>G GRCh38
NC_000002.11:g.234682997A>G , CM000664.1:g.234682997A>G GRCh37
NC_000002.10:g.234347736A>G NCBI36
NG_002601.2:g.189608A>G
NG_033238.1:g.19079A>G , LRG_733:g.19079A>G
NG_051337.1:g.3690A>G

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1421A>G XP_024308610.1:n.-1421A>G
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