Canonical Allele Identifier: CA381652023

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703875C>G (hg19) ; chr11:g.68936407C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936407C>G , CM000673.2:g.68936407C>G	GRCh38
NC_000011.9:g.68703875C>G , CM000673.1:g.68703875C>G	GRCh37
NC_000011.8:g.68460451C>G	NCBI36
NG_007976.1:g.37557C>G , LRG_250:g.37557C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1927C>G MANE Select	ENSP00000255078.4:p.Leu643Val
ENST00000674675.1:c.171C>G
ENST00000674878.1:c.171C>G
ENST00000674955.1:c.*644C>G	ENSP00000502463.1:n.*644C>G
ENST00000675118.1:c.1415C>G
ENST00000675389.1:n.202C>G
ENST00000675615.1:c.1927C>G	ENSP00000502413.1:p.Leu643Val
ENST00000675648.1:n.1302C>G
ENST00000675916.1:c.171C>G
ENST00000676173.1:n.2672C>G
ENST00000676182.1:c.358C>G
ENST00000676228.1:c.*1250C>G	ENSP00000502375.1:n.*1250C>G
ENST00000255078.7:c.1927C>G	ENSP00000255078.3:p.Leu643Val
ENST00000539064.5:n.1686C>G
ENST00000543739.5:n.920C>G
ENST00000545475.1:n.523C>G
NM_002180.2:c.1927C>G , LRG_250t1:c.1927C>G	NP_002171.2:p.Leu643Val
XM_005273974.2:c.916C>G	XP_005274031.1:p.Leu306Val
XM_005273975.2:c.799C>G	XP_005274032.1:p.Leu267Val
XM_011544994.1:c.694C>G	XP_011543296.1:p.Leu232Val
XR_949903.1:n.2029C>G
XM_005273975.3:c.799C>G	XP_005274032.1:p.Leu267Val
XM_017017669.2:c.916C>G	XP_016873158.1:p.Leu306Val
XM_017017670.2:c.916C>G	XP_016873159.1:p.Leu306Val
XR_949903.3:n.2025C>G
NM_002180.3:c.1927C>G MANE Select	NP_002171.2:p.Leu643Val