Canonical Allele Identifier: CA766294092
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1500482
MyVariant Identifiers: chr2:g.234683038C>A (hg19) chr2:g.233774392C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774392C>A , CM000664.2:g.233774392C>A GRCh38
NC_000002.11:g.234683038C>A , CM000664.1:g.234683038C>A GRCh37
NC_000002.10:g.234347777C>A NCBI36
NG_002601.2:g.189649C>A
NG_033238.1:g.19120C>A , LRG_733:g.19120C>A
NG_051337.1:g.3731C>A

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1380C>A XP_024308610.1:n.-1380C>A
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