Canonical Allele Identifier: CA381649666

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701277T>G (hg19) ; chr11:g.68933809T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933809T>G , CM000673.2:g.68933809T>G	GRCh38
NC_000011.9:g.68701277T>G , CM000673.1:g.68701277T>G	GRCh37
NC_000011.8:g.68457853T>G	NCBI36
NG_007976.1:g.34959T>G , LRG_250:g.34959T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1433T>G MANE Select	ENSP00000255078.4:p.Val478Gly
ENST00000674955.1:c.*150T>G	ENSP00000502463.1:n.*150T>G
ENST00000675118.1:c.921T>G
ENST00000675205.1:n.183+328T>G
ENST00000675615.1:c.1433T>G	ENSP00000502413.1:p.Val478Gly
ENST00000675648.1:n.808T>G
ENST00000675997.1:n.113-655T>G
ENST00000676173.1:n.2178T>G
ENST00000676228.1:c.*756T>G	ENSP00000502375.1:n.*756T>G
ENST00000255078.7:c.1433T>G	ENSP00000255078.3:p.Val478Gly
ENST00000537458.5:n.550T>G
ENST00000539064.5:n.1192T>G
ENST00000541229.5:n.128T>G
ENST00000543739.5:n.550T>G
NM_002180.2:c.1433T>G , LRG_250t1:c.1433T>G	NP_002171.2:p.Val478Gly
XM_005273974.2:c.422T>G	XP_005274031.1:p.Val141Gly
XM_005273975.2:c.305T>G	XP_005274032.1:p.Val102Gly
XM_011544994.1:c.200T>G	XP_011543296.1:p.Val67Gly
XR_949903.1:n.1535T>G
XM_005273975.3:c.305T>G	XP_005274032.1:p.Val102Gly
XM_017017669.2:c.422T>G	XP_016873158.1:p.Val141Gly
XM_017017670.2:c.422T>G	XP_016873159.1:p.Val141Gly
XM_017017671.2:c.1433T>G	XP_016873160.1:p.Val478Gly
XR_949903.3:n.1531T>G
NM_002180.3:c.1433T>G MANE Select	NP_002171.2:p.Val478Gly