Canonical Allele Identifier: CA381650118

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701339T>G (hg19) ; chr11:g.68933871T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933871T>G , CM000673.2:g.68933871T>G	GRCh38
NC_000011.9:g.68701339T>G , CM000673.1:g.68701339T>G	GRCh37
NC_000011.8:g.68457915T>G	NCBI36
NG_007976.1:g.35021T>G , LRG_250:g.35021T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1495T>G MANE Select	ENSP00000255078.4:p.Phe499Val
ENST00000674955.1:c.*212T>G	ENSP00000502463.1:n.*212T>G
ENST00000675118.1:c.983T>G
ENST00000675205.1:n.183+390T>G
ENST00000675615.1:c.1495T>G	ENSP00000502413.1:p.Phe499Val
ENST00000675648.1:n.870T>G
ENST00000675997.1:n.113-593T>G
ENST00000676173.1:n.2240T>G
ENST00000676228.1:c.*818T>G	ENSP00000502375.1:n.*818T>G
ENST00000255078.7:c.1495T>G	ENSP00000255078.3:p.Phe499Val
ENST00000537458.5:n.612T>G
ENST00000539064.5:n.1254T>G
ENST00000541229.5:n.190T>G
ENST00000543739.5:n.612T>G
NM_002180.2:c.1495T>G , LRG_250t1:c.1495T>G	NP_002171.2:p.Phe499Val
XM_005273974.2:c.484T>G	XP_005274031.1:p.Phe162Val
XM_005273975.2:c.367T>G	XP_005274032.1:p.Phe123Val
XM_011544994.1:c.262T>G	XP_011543296.1:p.Phe88Val
XR_949903.1:n.1597T>G
XM_005273975.3:c.367T>G	XP_005274032.1:p.Phe123Val
XM_017017669.2:c.484T>G	XP_016873158.1:p.Phe162Val
XM_017017670.2:c.484T>G	XP_016873159.1:p.Phe162Val
XM_017017671.2:c.1495T>G	XP_016873160.1:p.Phe499Val
XR_949903.3:n.1593T>G
NM_002180.3:c.1495T>G MANE Select	NP_002171.2:p.Phe499Val