Canonical Allele Identifier: CA11049533

Gene: MROH2A

Linked Data

• dbSNP Id: rs1500482
• gnomAD v2: 2-234683038-C-T
• gnomAD v3: 2-233774392-C-T
• gnomAD v4: 2-233774392-C-T
• MyVariant Identifiers: chr2:g.234683038C>T (hg19) ; chr2:g.233774392C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774392C>T , CM000664.2:g.233774392C>T	GRCh38
NC_000002.11:g.234683038C>T , CM000664.1:g.234683038C>T	GRCh37
NC_000002.10:g.234347777C>T	NCBI36
NG_002601.2:g.189649C>T
NG_033238.1:g.19120C>T , LRG_733:g.19120C>T
NG_051337.1:g.3731C>T

Transcript Alleles

HGVS	Amino-acid change
XM_024452842.1:c.-1380C>T	XP_024308610.1:n.-1380C>T