Canonical Allele Identifier: CA475280885

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704378T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936910T>G , CM000673.2:g.68936910T>G	GRCh38
NC_000011.9:g.68704378T>G , CM000673.1:g.68704378T>G	GRCh37
NC_000011.8:g.68460954T>G	NCBI36
NG_007976.1:g.38060T>G , LRG_250:g.38060T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2430T>G MANE Select	ENSP00000255078.4:p.Pro810=
ENST00000674675.1:c.588-13T>G
ENST00000674878.1:c.548-13T>G
ENST00000675118.1:c.1918T>G
ENST00000675389.1:n.705T>G
ENST00000675615.1:c.2430T>G	ENSP00000502413.1:p.Pro810=
ENST00000675648.1:n.1805T>G
ENST00000675916.1:c.674T>G
ENST00000676173.1:n.3175T>G
ENST00000676182.1:c.861T>G
ENST00000676228.1:c.*1753T>G	ENSP00000502375.1:n.*1753T>G
ENST00000255078.7:c.2430T>G	ENSP00000255078.3:p.Pro810=
ENST00000539064.5:n.2189T>G
ENST00000543739.5:n.1423T>G
NM_002180.2:c.2430T>G , LRG_250t1:c.2430T>G	NP_002171.2:p.Pro810=
XM_005273974.2:c.1419T>G	XP_005274031.1:p.Pro473=
XM_005273975.2:c.1302T>G	XP_005274032.1:p.Pro434=
XM_011544994.1:c.1197T>G	XP_011543296.1:p.Pro399=
XR_949903.1:n.2532T>G
XM_005273975.3:c.1302T>G	XP_005274032.1:p.Pro434=
XM_017017669.2:c.1419T>G	XP_016873158.1:p.Pro473=
XM_017017670.2:c.1419T>G	XP_016873159.1:p.Pro473=
XR_949903.3:n.2528T>G
NM_002180.3:c.2430T>G MANE Select	NP_002171.2:p.Pro810=