Canonical Allele Identifier: CA475279524
Gene: IGHMBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.68704051T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68936583T>A , CM000673.2:g.68936583T>A GRCh38
NC_000011.9:g.68704051T>A , CM000673.1:g.68704051T>A GRCh37
NC_000011.8:g.68460627T>A NCBI36
NG_007976.1:g.37733T>A , LRG_250:g.37733T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.2103T>A MANE Select ENSP00000255078.4:p.Ser701=
ENST00000674675.1:c.347T>A
ENST00000674878.1:c.347T>A
ENST00000674955.1:c.*820T>A ENSP00000502463.1:n.*820T>A
ENST00000675118.1:c.1591T>A
ENST00000675389.1:n.378T>A
ENST00000675615.1:c.2103T>A ENSP00000502413.1:p.Ser701=
ENST00000675648.1:n.1478T>A
ENST00000675916.1:c.347T>A
ENST00000676173.1:n.2848T>A
ENST00000676182.1:c.534T>A
ENST00000676228.1:c.*1426T>A ENSP00000502375.1:n.*1426T>A
ENST00000255078.7:c.2103T>A ENSP00000255078.3:p.Ser701=
ENST00000539064.5:n.1862T>A
ENST00000543739.5:n.1096T>A
NM_002180.2:c.2103T>A , LRG_250t1:c.2103T>A NP_002171.2:p.Ser701=
XM_005273974.2:c.1092T>A XP_005274031.1:p.Ser364=
XM_005273975.2:c.975T>A XP_005274032.1:p.Ser325=
XM_011544994.1:c.870T>A XP_011543296.1:p.Ser290=
XR_949903.1:n.2205T>A
XM_005273975.3:c.975T>A XP_005274032.1:p.Ser325=
XM_017017669.2:c.1092T>A XP_016873158.1:p.Ser364=
XM_017017670.2:c.1092T>A XP_016873159.1:p.Ser364=
XR_949903.3:n.2201T>A
NM_002180.3:c.2103T>A MANE Select NP_002171.2:p.Ser701=