Canonical Allele Identifier: CA381651673

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703786A>G (hg19) ; chr11:g.68936318A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936318A>G , CM000673.2:g.68936318A>G	GRCh38
NC_000011.9:g.68703786A>G , CM000673.1:g.68703786A>G	GRCh37
NC_000011.8:g.68460362A>G	NCBI36
NG_007976.1:g.37468A>G , LRG_250:g.37468A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1838A>G MANE Select	ENSP00000255078.4:p.Asp613Gly
ENST00000674675.1:c.82A>G
ENST00000674878.1:c.82A>G
ENST00000674955.1:c.*555A>G	ENSP00000502463.1:n.*555A>G
ENST00000675118.1:c.1326A>G
ENST00000675389.1:n.113A>G
ENST00000675615.1:c.1838A>G	ENSP00000502413.1:p.Asp613Gly
ENST00000675648.1:n.1213A>G
ENST00000675916.1:c.82A>G
ENST00000676173.1:n.2583A>G
ENST00000676182.1:c.269A>G
ENST00000676228.1:c.*1161A>G	ENSP00000502375.1:n.*1161A>G
ENST00000255078.7:c.1838A>G	ENSP00000255078.3:p.Asp613Gly
ENST00000539064.5:n.1597A>G
ENST00000541229.5:n.533A>G
ENST00000543739.5:n.831A>G
ENST00000545475.1:n.434A>G
NM_002180.2:c.1838A>G , LRG_250t1:c.1838A>G	NP_002171.2:p.Asp613Gly
XM_005273974.2:c.827A>G	XP_005274031.1:p.Asp276Gly
XM_005273975.2:c.710A>G	XP_005274032.1:p.Asp237Gly
XM_011544994.1:c.605A>G	XP_011543296.1:p.Asp202Gly
XR_949903.1:n.1940A>G
XM_005273975.3:c.710A>G	XP_005274032.1:p.Asp237Gly
XM_017017669.2:c.827A>G	XP_016873158.1:p.Asp276Gly
XM_017017670.2:c.827A>G	XP_016873159.1:p.Asp276Gly
XR_949903.3:n.1936A>G
NM_002180.3:c.1838A>G MANE Select	NP_002171.2:p.Asp613Gly