Canonical Allele Identifier: CA381647794

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68929325C>G , CM000673.2:g.68929325C>G	GRCh38
NC_000011.9:g.68696793C>G , CM000673.1:g.68696793C>G	GRCh37
NC_000011.8:g.68453369C>G	NCBI36
NG_007976.1:g.30475C>G , LRG_250:g.30475C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002180.3:c.1203C>G MANE Select	NP_002171.2:p.His401Gln
ENST00000255078.8:c.1203C>G MANE Select	ENSP00000255078.4:p.His401Gln
NM_002180.2:c.1203C>G , LRG_250t1:c.1203C>G	NP_002171.2:p.His401Gln
ENST00000255078.7:c.1203C>G	ENSP00000255078.3:p.His401Gln
ENST00000568742.1:n.313C>G
ENST00000674698.1:n.143C>G
ENST00000674745.1:c.368C>G	ENSP00000502738.1:n.368C>G
ENST00000674775.1:n.403C>G
ENST00000674955.1:c.1203C>G	ENSP00000502463.1:p.His401Gln
ENST00000675118.1:c.691C>G
ENST00000675305.1:c.523C>G	ENSP00000502365.1:n.523C>G
ENST00000675310.1:n.143C>G
ENST00000675493.1:n.364C>G
ENST00000675615.1:c.1203C>G	ENSP00000502413.1:p.His401Gln
ENST00000675648.1:n.578C>G
ENST00000675684.1:c.330C>G	ENSP00000502192.1:p.His110Gln
ENST00000675755.1:n.143C>G
ENST00000676083.1:n.143C>G
ENST00000676173.1:n.1247C>G
ENST00000676228.1:c.*526C>G	ENSP00000502375.1:n.*526C>G
ENST00000676240.1:n.143C>G
ENST00000676400.1:n.143C>G
XM_005273974.2:c.192C>G	XP_005274031.1:p.His64Gln
XM_005273976.1:c.1203C>G	XP_005274033.1:p.His401Gln
XM_005273976.2:c.1203C>G	XP_005274033.1:p.His401Gln
XM_017017669.2:c.192C>G	XP_016873158.1:p.His64Gln
XM_017017670.2:c.192C>G	XP_016873159.1:p.His64Gln
XM_017017671.2:c.1203C>G	XP_016873160.1:p.His401Gln
XR_247198.1:n.1305C>G
XR_949903.1:n.1305C>G
XR_949903.3:n.1301C>G