Canonical Allele Identifier: CA766294071
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1379211912
MyVariant Identifiers: chr2:g.234682997A>T (hg19) chr2:g.233774351A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XM_024452842.1:c.-1421A>T XP_024308610.1:n.-1421A>T
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