Canonical Allele Identifier: CA381649619

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701270C>G (hg19) ; chr11:g.68933802C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933802C>G , CM000673.2:g.68933802C>G	GRCh38
NC_000011.9:g.68701270C>G , CM000673.1:g.68701270C>G	GRCh37
NC_000011.8:g.68457846C>G	NCBI36
NG_007976.1:g.34952C>G , LRG_250:g.34952C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1426C>G MANE Select	ENSP00000255078.4:p.Pro476Ala
ENST00000674955.1:c.*143C>G	ENSP00000502463.1:n.*143C>G
ENST00000675118.1:c.914C>G
ENST00000675205.1:n.183+321C>G
ENST00000675615.1:c.1426C>G	ENSP00000502413.1:p.Pro476Ala
ENST00000675648.1:n.801C>G
ENST00000675997.1:n.113-662C>G
ENST00000676173.1:n.2171C>G
ENST00000676228.1:c.*749C>G	ENSP00000502375.1:n.*749C>G
ENST00000255078.7:c.1426C>G	ENSP00000255078.3:p.Pro476Ala
ENST00000537458.5:n.543C>G
ENST00000539064.5:n.1185C>G
ENST00000541229.5:n.121C>G
ENST00000543739.5:n.543C>G
NM_002180.2:c.1426C>G , LRG_250t1:c.1426C>G	NP_002171.2:p.Pro476Ala
XM_005273974.2:c.415C>G	XP_005274031.1:p.Pro139Ala
XM_005273975.2:c.298C>G	XP_005274032.1:p.Pro100Ala
XM_011544994.1:c.193C>G	XP_011543296.1:p.Pro65Ala
XR_949903.1:n.1528C>G
XM_005273975.3:c.298C>G	XP_005274032.1:p.Pro100Ala
XM_017017669.2:c.415C>G	XP_016873158.1:p.Pro139Ala
XM_017017670.2:c.415C>G	XP_016873159.1:p.Pro139Ala
XM_017017671.2:c.1426C>G	XP_016873160.1:p.Pro476Ala
XR_949903.3:n.1524C>G
NM_002180.3:c.1426C>G MANE Select	NP_002171.2:p.Pro476Ala