Canonical Allele Identifier: CA766294088
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1249814985
MyVariant Identifiers: chr2:g.234683035T>C (hg19) chr2:g.233774389T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774389T>C , CM000664.2:g.233774389T>C GRCh38
NC_000002.11:g.234683035T>C , CM000664.1:g.234683035T>C GRCh37
NC_000002.10:g.234347774T>C NCBI36
NG_002601.2:g.189646T>C
NG_033238.1:g.19117T>C , LRG_733:g.19117T>C
NG_051337.1:g.3728T>C

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1383T>C XP_024308610.1:n.-1383T>C
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