Canonical Allele Identifier: CA360550686

Gene: RGMB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.98774153C>G , CM000667.2:g.98774153C>G	GRCh38
NC_000005.9:g.98109857C>G , CM000667.1:g.98109857C>G	GRCh37
NC_000005.8:g.98137757C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001366508.1:c.83C>G MANE Select	NP_001353437.1:p.Pro28Arg
ENST00000513185.3:c.83C>G MANE Select	ENSP00000423256.1:p.Pro28Arg
NM_001012761.2:c.206C>G	NP_001012779.2:p.Pro69Arg
NM_001012761.3:c.206C>G	NP_001012779.2:p.Pro69Arg
NM_001366509.1:c.206C>G	NP_001353438.1:p.Pro69Arg
NM_001366510.1:c.206C>G	NP_001353439.1:p.Pro69Arg
NM_001366511.1:c.203C>G	NP_001353440.1:p.Pro68Arg
ENST00000308234.11:c.206C>G	ENSP00000308219.7:p.Pro69Arg
ENST00000434027.2:n.854C>G
ENST00000504776.5:n.487C>G
ENST00000513185.1:c.83C>G	ENSP00000423256.1:p.Pro28Arg
XM_005271966.2:c.203C>G	XP_005272023.1:p.Pro68Arg
XM_011543345.1:c.206C>G	XP_011541647.1:p.Pro69Arg
XM_011543345.2:c.206C>G	XP_011541647.1:p.Pro69Arg
XM_011543347.1:c.305C>G	XP_011541649.1:p.Pro102Arg
XM_011543347.3:c.206C>G	XP_011541649.2:p.Pro69Arg