Canonical Allele Identifier: CA381644555
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68914996T>G , CM000673.2:g.68914996T>G GRCh38
NC_000011.9:g.68682464T>G , CM000673.1:g.68682464T>G GRCh37
NC_000011.8:g.68439040T>G NCBI36
NG_007976.1:g.16146T>G , LRG_250:g.16146T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.885T>G MANE Select ENSP00000255078.4:p.Asp295Glu
ENST00000539224.2:c.1014T>G
ENST00000674955.1:c.885T>G ENSP00000502463.1:p.Asp295Glu
ENST00000675118.1:c.232T>G
ENST00000675119.1:c.174T>G ENSP00000501861.1:p.Asp58Glu
ENST00000675305.1:c.174T>G ENSP00000502365.1:p.Asp58Glu
ENST00000675464.1:c.174T>G ENSP00000502650.1:p.Asp58Glu
ENST00000675615.1:c.885T>G ENSP00000502413.1:p.Asp295Glu
ENST00000675683.1:c.272T>G
ENST00000676173.1:n.929T>G
ENST00000676228.1:c.*208T>G ENSP00000502375.1:n.*208T>G
ENST00000676239.1:n.199T>G
ENST00000255078.7:c.885T>G ENSP00000255078.3:p.Asp295Glu
NM_002180.2:c.885T>G , LRG_250t1:c.885T>G NP_002171.2:p.Asp295Glu
XM_005273974.2:c.-127T>G XP_005274031.1:n.-127T>G
XM_005273976.1:c.885T>G XP_005274033.1:p.Asp295Glu
XR_247198.1:n.987T>G
XR_949903.1:n.987T>G
XM_005273976.2:c.885T>G XP_005274033.1:p.Asp295Glu
XM_017017669.2:c.-127T>G XP_016873158.1:n.-127T>G
XM_017017670.2:c.-127T>G XP_016873159.1:n.-127T>G
XM_017017671.2:c.885T>G XP_016873160.1:p.Asp295Glu
XR_949903.3:n.983T>G
NM_002180.3:c.885T>G MANE Select NP_002171.2:p.Asp295Glu