Canonical Allele Identifier: CA123695159

Gene: RGMB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.98774155C>A , CM000667.2:g.98774155C>A	GRCh38
NC_000005.9:g.98109859C>A , CM000667.1:g.98109859C>A	GRCh37
NC_000005.8:g.98137759C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513185.3:c.85C>A MANE Select	ENSP00000423256.1:p.Pro29Thr
ENST00000308234.11:c.208C>A	ENSP00000308219.7:p.Pro70Thr
ENST00000434027.2:n.856C>A
ENST00000504776.5:n.489C>A
ENST00000513185.1:c.85C>A	ENSP00000423256.1:p.Pro29Thr
NM_001012761.2:c.208C>A	NP_001012779.2:p.Pro70Thr
XM_005271966.2:c.205C>A	XP_005272023.1:p.Pro69Thr
XM_011543345.1:c.208C>A	XP_011541647.1:p.Pro70Thr
XM_011543347.1:c.307C>A	XP_011541649.1:p.Pro103Thr
NM_001366508.1:c.85C>A MANE Select	NP_001353437.1:p.Pro29Thr
NM_001366509.1:c.208C>A	NP_001353438.1:p.Pro70Thr
NM_001366510.1:c.208C>A	NP_001353439.1:p.Pro70Thr
NM_001366511.1:c.205C>A	NP_001353440.1:p.Pro69Thr
XM_011543345.2:c.208C>A	XP_011541647.1:p.Pro70Thr
XM_011543347.3:c.208C>A	XP_011541649.2:p.Pro70Thr
NM_001012761.3:c.208C>A	NP_001012779.2:p.Pro70Thr