Canonical Allele Identifier: CA475279681

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704072T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936604T>G , CM000673.2:g.68936604T>G	GRCh38
NC_000011.9:g.68704072T>G , CM000673.1:g.68704072T>G	GRCh37
NC_000011.8:g.68460648T>G	NCBI36
NG_007976.1:g.37754T>G , LRG_250:g.37754T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2124T>G MANE Select	ENSP00000255078.4:p.Ser708=
ENST00000674675.1:c.368T>G
ENST00000674878.1:c.368T>G
ENST00000674955.1:c.*841T>G	ENSP00000502463.1:n.*841T>G
ENST00000675118.1:c.1612T>G
ENST00000675389.1:n.399T>G
ENST00000675615.1:c.2124T>G	ENSP00000502413.1:p.Ser708=
ENST00000675648.1:n.1499T>G
ENST00000675916.1:c.368T>G
ENST00000676173.1:n.2869T>G
ENST00000676182.1:c.555T>G
ENST00000676228.1:c.*1447T>G	ENSP00000502375.1:n.*1447T>G
ENST00000255078.7:c.2124T>G	ENSP00000255078.3:p.Ser708=
ENST00000539064.5:n.1883T>G
ENST00000543739.5:n.1117T>G
NM_002180.2:c.2124T>G , LRG_250t1:c.2124T>G	NP_002171.2:p.Ser708=
XM_005273974.2:c.1113T>G	XP_005274031.1:p.Ser371=
XM_005273975.2:c.996T>G	XP_005274032.1:p.Ser332=
XM_011544994.1:c.891T>G	XP_011543296.1:p.Ser297=
XR_949903.1:n.2226T>G
XM_005273975.3:c.996T>G	XP_005274032.1:p.Ser332=
XM_017017669.2:c.1113T>G	XP_016873158.1:p.Ser371=
XM_017017670.2:c.1113T>G	XP_016873159.1:p.Ser371=
XR_949903.3:n.2222T>G
NM_002180.3:c.2124T>G MANE Select	NP_002171.2:p.Ser708=