Canonical Allele Identifier: CA6154059
Gene: IGHMBP2 HGNC NCBI

Linked Data

dbSNP Id: rs147674615

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68939671T>A , CM000673.2:g.68939671T>A GRCh38
NC_000011.9:g.68707139T>A , CM000673.1:g.68707139T>A GRCh37
NC_000011.8:g.68463715T>A NCBI36
NG_007976.1:g.40821T>A , LRG_250:g.40821T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.2922T>A MANE Select ENSP00000255078.4:p.Asp974Glu
ENST00000675118.1:c.2410T>A
ENST00000675615.1:c.*121T>A ENSP00000502413.1:n.*121T>A
ENST00000675648.1:n.2484T>A
ENST00000675916.1:c.1353T>A
ENST00000676173.1:n.3667T>A
ENST00000255078.7:c.2922T>A ENSP00000255078.3:p.Asp974Glu
ENST00000543739.5:n.1915T>A
ENST00000544521.1:n.753T>A
NM_002180.2:c.2922T>A , LRG_250t1:c.2922T>A NP_002171.2:p.Asp974Glu
XM_005273974.2:c.1911T>A XP_005274031.1:p.Asp637Glu
XM_005273975.2:c.1794T>A XP_005274032.1:p.Asp598Glu
XM_011544994.1:c.1689T>A XP_011543296.1:p.Asp563Glu
XR_949903.1:n.3211T>A
XM_005273975.3:c.1794T>A XP_005274032.1:p.Asp598Glu
XM_017017669.2:c.1911T>A XP_016873158.1:p.Asp637Glu
XM_017017670.2:c.1911T>A XP_016873159.1:p.Asp637Glu
XR_949903.3:n.3207T>A
NM_002180.3:c.2922T>A MANE Select NP_002171.2:p.Asp974Glu