Canonical Allele Identifier: CA766294063
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1316192715
MyVariant Identifiers: chr2:g.234682986G>A (hg19) chr2:g.233774340G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774340G>A , CM000664.2:g.233774340G>A GRCh38
NC_000002.11:g.234682986G>A , CM000664.1:g.234682986G>A GRCh37
NC_000002.10:g.234347725G>A NCBI36
NG_002601.2:g.189597G>A
NG_033238.1:g.19068G>A , LRG_733:g.19068G>A
NG_051337.1:g.3679G>A

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1432G>A XP_024308610.1:n.-1432G>A
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