Canonical Allele Identifier: CA766294117

Gene: MROH2A

Linked Data

• dbSNP Id: rs1219854396
• MyVariant Identifiers: chr2:g.234683136C>G (hg19) ; chr2:g.233774490C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774490C>G , CM000664.2:g.233774490C>G	GRCh38
NC_000002.11:g.234683136C>G , CM000664.1:g.234683136C>G	GRCh37
NC_000002.10:g.234347875C>G	NCBI36
NG_002601.2:g.189747C>G
NG_033238.1:g.19218C>G , LRG_733:g.19218C>G
NG_051337.1:g.3829C>G

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1282C>G	XP_024308610.1:n.-1282C>G