Canonical Allele Identifier: CA381649473

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68700945C>G (hg19) ; chr11:g.68933477C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933477C>G , CM000673.2:g.68933477C>G	GRCh38
NC_000011.9:g.68700945C>G , CM000673.1:g.68700945C>G	GRCh37
NC_000011.8:g.68457521C>G	NCBI36
NG_007976.1:g.34627C>G , LRG_250:g.34627C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1414C>G MANE Select	ENSP00000255078.4:p.Leu472Val
ENST00000536803.2:n.325C>G
ENST00000674955.1:c.*131C>G	ENSP00000502463.1:n.*131C>G
ENST00000675118.1:c.902C>G
ENST00000675205.1:n.179C>G
ENST00000675310.1:n.551C>G
ENST00000675615.1:c.1414C>G	ENSP00000502413.1:p.Leu472Val
ENST00000675648.1:n.789C>G
ENST00000675997.1:n.113-987C>G
ENST00000676149.1:n.488C>G
ENST00000676173.1:n.2159C>G
ENST00000676228.1:c.*737C>G	ENSP00000502375.1:n.*737C>G
ENST00000255078.7:c.1414C>G	ENSP00000255078.3:p.Leu472Val
ENST00000537458.5:n.531C>G
ENST00000539064.5:n.1173C>G
ENST00000543739.5:n.531C>G
NM_002180.2:c.1414C>G , LRG_250t1:c.1414C>G	NP_002171.2:p.Leu472Val
XM_005273974.2:c.403C>G	XP_005274031.1:p.Leu135Val
XM_005273975.2:c.286C>G	XP_005274032.1:p.Leu96Val
XM_011544994.1:c.181C>G	XP_011543296.1:p.Leu61Val
XR_949903.1:n.1516C>G
XM_005273975.3:c.286C>G	XP_005274032.1:p.Leu96Val
XM_017017669.2:c.403C>G	XP_016873158.1:p.Leu135Val
XM_017017670.2:c.403C>G	XP_016873159.1:p.Leu135Val
XM_017017671.2:c.1414C>G	XP_016873160.1:p.Leu472Val
XR_949903.3:n.1512C>G
NM_002180.3:c.1414C>G MANE Select	NP_002171.2:p.Leu472Val