Canonical Allele Identifier: CA766294065

Gene: MROH2A

Linked Data

• dbSNP Id: rs1304383870
• MyVariant Identifiers: chr2:g.234682990_234682991del (hg19) ; chr2:g.233774344_233774345del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233774346_233774347del , CM000664.2:g.233774346_233774347del	GRCh38
NC_000002.11:g.234682992_234682993del , CM000664.1:g.234682992_234682993del	GRCh37
NC_000002.10:g.234347731_234347732del	NCBI36
NG_002601.2:g.189603_189604del
NG_033238.1:g.19074_19075del , LRG_733:g.19074_19075del
NG_051337.1:g.3685_3686del

Transcript Alleles

HGVS	Amino-acid Change
XM_024452842.1:c.-1426_-1425del	XP_024308610.1:n.-1426_-1425del