Canonical Allele Identifier: CA475204209

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68936241-A-G
• MyVariant Identifiers: chr11:g.68703709A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936241A>G , CM000673.2:g.68936241A>G	GRCh38
NC_000011.9:g.68703709A>G , CM000673.1:g.68703709A>G	GRCh37
NC_000011.8:g.68460285A>G	NCBI36
NG_007976.1:g.37391A>G , LRG_250:g.37391A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1761A>G MANE Select	ENSP00000255078.4:p.Glu587=
ENST00000674675.1:c.5A>G
ENST00000674878.1:c.5A>G
ENST00000674955.1:c.*478A>G	ENSP00000502463.1:n.*478A>G
ENST00000675118.1:c.1249A>G
ENST00000675389.1:n.36A>G
ENST00000675615.1:c.1761A>G	ENSP00000502413.1:p.Glu587=
ENST00000675648.1:n.1136A>G
ENST00000675916.1:c.5A>G
ENST00000676173.1:n.2506A>G
ENST00000676182.1:c.192A>G
ENST00000676228.1:c.*1084A>G	ENSP00000502375.1:n.*1084A>G
ENST00000255078.7:c.1761A>G	ENSP00000255078.3:p.Glu587=
ENST00000539064.5:n.1520A>G
ENST00000541229.5:n.456A>G
ENST00000543739.5:n.754A>G
ENST00000545475.1:n.357A>G
NM_002180.2:c.1761A>G , LRG_250t1:c.1761A>G	NP_002171.2:p.Glu587=
XM_005273974.2:c.750A>G	XP_005274031.1:p.Glu250=
XM_005273975.2:c.633A>G	XP_005274032.1:p.Glu211=
XM_011544994.1:c.528A>G	XP_011543296.1:p.Glu176=
XR_949903.1:n.1863A>G
XM_005273975.3:c.633A>G	XP_005274032.1:p.Glu211=
XM_017017669.2:c.750A>G	XP_016873158.1:p.Glu250=
XM_017017670.2:c.750A>G	XP_016873159.1:p.Glu250=
XR_949903.3:n.1859A>G
NM_002180.3:c.1761A>G MANE Select	NP_002171.2:p.Glu587=