Canonical Allele Identifier: CA766294056
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1202918379
gnomAD v3: 2-233774303-C-G
gnomAD v4: 2-233774303-C-G
MyVariant Identifiers: chr2:g.234682949C>G (hg19) chr2:g.233774303C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774303C>G , CM000664.2:g.233774303C>G GRCh38
NC_000002.11:g.234682949C>G , CM000664.1:g.234682949C>G GRCh37
NC_000002.10:g.234347688C>G NCBI36
NG_002601.2:g.189560C>G
NG_033238.1:g.19031C>G , LRG_733:g.19031C>G
NG_051337.1:g.3642C>G

Transcript Alleles

HGVS Amino-acid change
XM_024452842.1:c.-1469C>G XP_024308610.1:n.-1469C>G
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