Canonical Allele Identifier: CA475279023

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68936499-C-G
• MyVariant Identifiers: chr11:g.68703967C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936499C>G , CM000673.2:g.68936499C>G	GRCh38
NC_000011.9:g.68703967C>G , CM000673.1:g.68703967C>G	GRCh37
NC_000011.8:g.68460543C>G	NCBI36
NG_007976.1:g.37649C>G , LRG_250:g.37649C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2019C>G MANE Select	ENSP00000255078.4:p.Thr673=
ENST00000674675.1:c.263C>G
ENST00000674878.1:c.263C>G
ENST00000674955.1:c.*736C>G	ENSP00000502463.1:n.*736C>G
ENST00000675118.1:c.1507C>G
ENST00000675389.1:n.294C>G
ENST00000675615.1:c.2019C>G	ENSP00000502413.1:p.Thr673=
ENST00000675648.1:n.1394C>G
ENST00000675916.1:c.263C>G
ENST00000676173.1:n.2764C>G
ENST00000676182.1:c.450C>G
ENST00000676228.1:c.*1342C>G	ENSP00000502375.1:n.*1342C>G
ENST00000255078.7:c.2019C>G	ENSP00000255078.3:p.Thr673=
ENST00000539064.5:n.1778C>G
ENST00000543739.5:n.1012C>G
NM_002180.2:c.2019C>G , LRG_250t1:c.2019C>G	NP_002171.2:p.Thr673=
XM_005273974.2:c.1008C>G	XP_005274031.1:p.Thr336=
XM_005273975.2:c.891C>G	XP_005274032.1:p.Thr297=
XM_011544994.1:c.786C>G	XP_011543296.1:p.Thr262=
XR_949903.1:n.2121C>G
XM_005273975.3:c.891C>G	XP_005274032.1:p.Thr297=
XM_017017669.2:c.1008C>G	XP_016873158.1:p.Thr336=
XM_017017670.2:c.1008C>G	XP_016873159.1:p.Thr336=
XR_949903.3:n.2117C>G
NM_002180.3:c.2019C>G MANE Select	NP_002171.2:p.Thr673=