Canonical Allele Identifier: CA381653429

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704319G>A (hg19) ; chr11:g.68936851G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936851G>A , CM000673.2:g.68936851G>A	GRCh38
NC_000011.9:g.68704319G>A , CM000673.1:g.68704319G>A	GRCh37
NC_000011.8:g.68460895G>A	NCBI36
NG_007976.1:g.38001G>A , LRG_250:g.38001G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2371G>A MANE Select	ENSP00000255078.4:p.Ala791Thr
ENST00000674675.1:c.587+28G>A
ENST00000674878.1:c.547+68G>A
ENST00000674955.1:c.*1088G>A	ENSP00000502463.1:n.*1088G>A
ENST00000675118.1:c.1859G>A
ENST00000675389.1:n.646G>A
ENST00000675615.1:c.2371G>A	ENSP00000502413.1:p.Ala791Thr
ENST00000675648.1:n.1746G>A
ENST00000675916.1:c.615G>A
ENST00000676173.1:n.3116G>A
ENST00000676182.1:c.802G>A
ENST00000676228.1:c.*1694G>A	ENSP00000502375.1:n.*1694G>A
ENST00000255078.7:c.2371G>A	ENSP00000255078.3:p.Ala791Thr
ENST00000539064.5:n.2130G>A
ENST00000543739.5:n.1364G>A
NM_002180.2:c.2371G>A , LRG_250t1:c.2371G>A	NP_002171.2:p.Ala791Thr
XM_005273974.2:c.1360G>A	XP_005274031.1:p.Ala454Thr
XM_005273975.2:c.1243G>A	XP_005274032.1:p.Ala415Thr
XM_011544994.1:c.1138G>A	XP_011543296.1:p.Ala380Thr
XR_949903.1:n.2473G>A
XM_005273975.3:c.1243G>A	XP_005274032.1:p.Ala415Thr
XM_017017669.2:c.1360G>A	XP_016873158.1:p.Ala454Thr
XM_017017670.2:c.1360G>A	XP_016873159.1:p.Ala454Thr
XR_949903.3:n.2469G>A
NM_002180.3:c.2371G>A MANE Select	NP_002171.2:p.Ala791Thr