Canonical Allele Identifier: CA381644251

Gene: IGHMBP2

Linked Data

• ClinVar Variation Id: 917017
• ClinVar RCV Id: RCV001173348 ; RCV002559661
• dbSNP Id: rs1858584931
• MyVariant Identifiers: chr11:g.68682307C>G (hg19) ; chr11:g.68914839C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914839C>G , CM000673.2:g.68914839C>G	GRCh38
NC_000011.9:g.68682307C>G , CM000673.1:g.68682307C>G	GRCh37
NC_000011.8:g.68438883C>G	NCBI36
NG_007976.1:g.15989C>G , LRG_250:g.15989C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.728C>G MANE Select	ENSP00000255078.4:p.Pro243Arg
ENST00000539224.2:c.857C>G
ENST00000674955.1:c.728C>G	ENSP00000502463.1:p.Pro243Arg
ENST00000675118.1:c.75C>G
ENST00000675119.1:c.17C>G	ENSP00000501861.1:p.Pro6Arg
ENST00000675305.1:c.17C>G	ENSP00000502365.1:p.Pro6Arg
ENST00000675464.1:c.17C>G	ENSP00000502650.1:p.Pro6Arg
ENST00000675615.1:c.728C>G	ENSP00000502413.1:p.Pro243Arg
ENST00000675683.1:c.115C>G
ENST00000676173.1:n.772C>G
ENST00000676228.1:c.*51C>G	ENSP00000502375.1:n.*51C>G
ENST00000676239.1:n.42C>G
ENST00000255078.7:c.728C>G	ENSP00000255078.3:p.Pro243Arg
ENST00000539224.1:c.*51C>G	ENSP00000440465.1:n.*51C>G
NM_002180.2:c.728C>G , LRG_250t1:c.728C>G	NP_002171.2:p.Pro243Arg
XM_005273974.2:c.-284C>G	XP_005274031.1:n.-284C>G
XM_005273976.1:c.728C>G	XP_005274033.1:p.Pro243Arg
XR_247198.1:n.830C>G
XR_949903.1:n.830C>G
XM_005273976.2:c.728C>G	XP_005274033.1:p.Pro243Arg
XM_017017669.2:c.-284C>G	XP_016873158.1:n.-284C>G
XM_017017670.2:c.-284C>G	XP_016873159.1:n.-284C>G
XM_017017671.2:c.728C>G	XP_016873160.1:p.Pro243Arg
XR_949903.3:n.826C>G
NM_002180.3:c.728C>G MANE Select	NP_002171.2:p.Pro243Arg