Canonical Allele Identifier: CA381652850
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68936602T>A , CM000673.2:g.68936602T>A GRCh38
NC_000011.9:g.68704070T>A , CM000673.1:g.68704070T>A GRCh37
NC_000011.8:g.68460646T>A NCBI36
NG_007976.1:g.37752T>A , LRG_250:g.37752T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.2122T>A MANE Select ENSP00000255078.4:p.Ser708Thr
ENST00000674675.1:c.366T>A
ENST00000674878.1:c.366T>A
ENST00000674955.1:c.*839T>A ENSP00000502463.1:n.*839T>A
ENST00000675118.1:c.1610T>A
ENST00000675389.1:n.397T>A
ENST00000675615.1:c.2122T>A ENSP00000502413.1:p.Ser708Thr
ENST00000675648.1:n.1497T>A
ENST00000675916.1:c.366T>A
ENST00000676173.1:n.2867T>A
ENST00000676182.1:c.553T>A
ENST00000676228.1:c.*1445T>A ENSP00000502375.1:n.*1445T>A
ENST00000255078.7:c.2122T>A ENSP00000255078.3:p.Ser708Thr
ENST00000539064.5:n.1881T>A
ENST00000543739.5:n.1115T>A
NM_002180.2:c.2122T>A , LRG_250t1:c.2122T>A NP_002171.2:p.Ser708Thr
XM_005273974.2:c.1111T>A XP_005274031.1:p.Ser371Thr
XM_005273975.2:c.994T>A XP_005274032.1:p.Ser332Thr
XM_011544994.1:c.889T>A XP_011543296.1:p.Ser297Thr
XR_949903.1:n.2224T>A
XM_005273975.3:c.994T>A XP_005274032.1:p.Ser332Thr
XM_017017669.2:c.1111T>A XP_016873158.1:p.Ser371Thr
XM_017017670.2:c.1111T>A XP_016873159.1:p.Ser371Thr
XR_949903.3:n.2220T>A
NM_002180.3:c.2122T>A MANE Select NP_002171.2:p.Ser708Thr