Canonical Allele Identifier: CA67601264
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs924208162
gnomAD v2: 2-234683014-A-G
gnomAD v3: 2-233774368-A-G
gnomAD v4: 2-233774368-A-G
MyVariant Identifiers: chr2:g.234683014A>G (hg19) chr2:g.233774368A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774368A>G , CM000664.2:g.233774368A>G GRCh38
NC_000002.11:g.234683014A>G , CM000664.1:g.234683014A>G GRCh37
NC_000002.10:g.234347753A>G NCBI36
NG_002601.2:g.189625A>G
NG_033238.1:g.19096A>G , LRG_733:g.19096A>G
NG_051337.1:g.3707A>G

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1404A>G XP_024308610.1:n.-1404A>G
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