Canonical Allele Identifier: CA939177896
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68915184_68915185insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.2:g.68915184_68915185insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000011.9:g.68682652_68682653insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000673.1:g.68682652_68682653insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000011.8:g.68439228_68439229insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_007976.1:g.16334_16335insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250:g.16334_16335insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000255078.4:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000539224.2:c.1041+161_1041+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000502463.1:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675118.1:c.259+161_259+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+161_201+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000501861.1:n.201+161_201+162insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675305.1:c.201+161_201+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000502365.1:n.201+161_201+162insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675464.1:c.195+167_195+168insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000502650.1:n.195+167_195+168insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675615.1:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000502413.1:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTT...
ENST00000675683.1:c.299+161_299+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+161_956+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+161_*235+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000502375.1:n.*235+161_*235+162insATTTTTTTTTTTTTTTTTTTT...
ENST00000255078.7:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000255078.3:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTT...
NM_002180.2:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_002171.2:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005273974.2:c.-100+161_-100+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005274031.1:n.-100+161_-100+162insATTTTTTTTTTTTTTTTTTTTTTT...
XM_005273976.1:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005274033.1:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTT...
XR_247198.1:n.1014+161_1014+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_949903.1:n.1014+161_1014+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005273976.2:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005274033.1:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTT...
XM_017017669.2:c.-100+161_-100+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016873158.1:n.-100+161_-100+162insATTTTTTTTTTTTTTTTTTTTTTT...
XM_017017670.2:c.-100+161_-100+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016873159.1:n.-100+161_-100+162insATTTTTTTTTTTTTTTTTTTTTTT...
XM_017017671.2:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016873160.1:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTT...
XR_949903.3:n.1010+161_1010+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_002180.3:c.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_002171.2:n.912+161_912+162insATTTTTTTTTTTTTTTTTTTTTTTTTTTT...