Canonical Allele Identifier: CA475280900

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704402T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936934T>G , CM000673.2:g.68936934T>G	GRCh38
NC_000011.9:g.68704402T>G , CM000673.1:g.68704402T>G	GRCh37
NC_000011.8:g.68460978T>G	NCBI36
NG_007976.1:g.38084T>G , LRG_250:g.38084T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2454T>G MANE Select	ENSP00000255078.4:p.Pro818=
ENST00000674675.1:c.599T>G
ENST00000674878.1:c.559T>G
ENST00000675118.1:c.1942T>G
ENST00000675389.1:n.729T>G
ENST00000675615.1:c.2454T>G	ENSP00000502413.1:p.Pro818=
ENST00000675648.1:n.1829T>G
ENST00000675916.1:c.698T>G
ENST00000676173.1:n.3199T>G
ENST00000676182.1:c.885T>G
ENST00000676228.1:c.*1777T>G	ENSP00000502375.1:n.*1777T>G
ENST00000255078.7:c.2454T>G	ENSP00000255078.3:p.Pro818=
ENST00000539064.5:n.2213T>G
ENST00000543739.5:n.1447T>G
NM_002180.2:c.2454T>G , LRG_250t1:c.2454T>G	NP_002171.2:p.Pro818=
XM_005273974.2:c.1443T>G	XP_005274031.1:p.Pro481=
XM_005273975.2:c.1326T>G	XP_005274032.1:p.Pro442=
XM_011544994.1:c.1221T>G	XP_011543296.1:p.Pro407=
XR_949903.1:n.2556T>G
XM_005273975.3:c.1326T>G	XP_005274032.1:p.Pro442=
XM_017017669.2:c.1443T>G	XP_016873158.1:p.Pro481=
XM_017017670.2:c.1443T>G	XP_016873159.1:p.Pro481=
XR_949903.3:n.2552T>G
NM_002180.3:c.2454T>G MANE Select	NP_002171.2:p.Pro818=