Canonical Allele Identifier: CA475279001

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68936484-A-G
• MyVariant Identifiers: chr11:g.68703952A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936484A>G , CM000673.2:g.68936484A>G	GRCh38
NC_000011.9:g.68703952A>G , CM000673.1:g.68703952A>G	GRCh37
NC_000011.8:g.68460528A>G	NCBI36
NG_007976.1:g.37634A>G , LRG_250:g.37634A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2004A>G MANE Select	ENSP00000255078.4:p.Gly668=
ENST00000674675.1:c.248A>G
ENST00000674878.1:c.248A>G
ENST00000674955.1:c.*721A>G	ENSP00000502463.1:n.*721A>G
ENST00000675118.1:c.1492A>G
ENST00000675389.1:n.279A>G
ENST00000675615.1:c.2004A>G	ENSP00000502413.1:p.Gly668=
ENST00000675648.1:n.1379A>G
ENST00000675916.1:c.248A>G
ENST00000676173.1:n.2749A>G
ENST00000676182.1:c.435A>G
ENST00000676228.1:c.*1327A>G	ENSP00000502375.1:n.*1327A>G
ENST00000255078.7:c.2004A>G	ENSP00000255078.3:p.Gly668=
ENST00000539064.5:n.1763A>G
ENST00000543739.5:n.997A>G
NM_002180.2:c.2004A>G , LRG_250t1:c.2004A>G	NP_002171.2:p.Gly668=
XM_005273974.2:c.993A>G	XP_005274031.1:p.Gly331=
XM_005273975.2:c.876A>G	XP_005274032.1:p.Gly292=
XM_011544994.1:c.771A>G	XP_011543296.1:p.Gly257=
XR_949903.1:n.2106A>G
XM_005273975.3:c.876A>G	XP_005274032.1:p.Gly292=
XM_017017669.2:c.993A>G	XP_016873158.1:p.Gly331=
XM_017017670.2:c.993A>G	XP_016873159.1:p.Gly331=
XR_949903.3:n.2102A>G
NM_002180.3:c.2004A>G MANE Select	NP_002171.2:p.Gly668=