Canonical Allele Identifier: CA1043573562
Gene: MROH2A HGNC NCBI

Linked Data

dbSNP Id: rs1700629133
gnomAD v3: 2-233774309-T-C
gnomAD v4: 2-233774309-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233774309T>C , CM000664.2:g.233774309T>C GRCh38
NC_000002.11:g.234682955T>C , CM000664.1:g.234682955T>C GRCh37
NC_000002.10:g.234347694T>C NCBI36
NG_002601.2:g.189566T>C
NG_033238.1:g.19037T>C , LRG_733:g.19037T>C
NG_051337.1:g.3648T>C

Transcript Alleles

HGVS Amino-acid Change
XM_024452842.1:c.-1463T>C XP_024308610.1:n.-1463T>C
Search 100 bp 5'
Search 100 bp 3'