Canonical Allele Identifier: CA67601288

Gene: MROH2A

Linked Data

• dbSNP Id: rs948180798
• gnomAD v3: 2-233774393-T-C
• gnomAD v4: 2-233774393-T-C
• MyVariant Identifiers: chr2:g.234683039T>C (hg19) ; chr2:g.233774393T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774393T>C , CM000664.2:g.233774393T>C	GRCh38
NC_000002.11:g.234683039T>C , CM000664.1:g.234683039T>C	GRCh37
NC_000002.10:g.234347778T>C	NCBI36
NG_002601.2:g.189650T>C
NG_033238.1:g.19121T>C , LRG_733:g.19121T>C
NG_051337.1:g.3732T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1379T>C	XP_024308610.1:n.-1379T>C