Canonical Allele Identifier: CA2614746116
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68915141_68915142insGT , CM000673.2:g.68915141_68915142insGT GRCh38
NC_000011.9:g.68682609_68682610insGT , CM000673.1:g.68682609_68682610insGT GRCh37
NC_000011.8:g.68439185_68439186insGT NCBI36
NG_007976.1:g.16291_16292insGT , LRG_250:g.16291_16292insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.912+118_912+119insGT MANE Select ENSP00000255078.4:n.912+118_912+119insGT
ENST00000539224.2:c.1041+118_1041+119insGT
ENST00000674955.1:c.912+118_912+119insGT ENSP00000502463.1:n.912+118_912+119insGT
ENST00000675118.1:c.259+118_259+119insGT
ENST00000675119.1:c.201+118_201+119insGT ENSP00000501861.1:n.201+118_201+119insGT
ENST00000675305.1:c.201+118_201+119insGT ENSP00000502365.1:n.201+118_201+119insGT
ENST00000675464.1:c.195+124_195+125insGT ENSP00000502650.1:n.195+124_195+125insGT
ENST00000675615.1:c.912+118_912+119insGT ENSP00000502413.1:n.912+118_912+119insGT
ENST00000675683.1:c.299+118_299+119insGT
ENST00000676173.1:n.956+118_956+119insGT
ENST00000676228.1:c.*235+118_*235+119insGT ENSP00000502375.1:n.*235+118_*235+119insGT
ENST00000255078.7:c.912+118_912+119insGT ENSP00000255078.3:n.912+118_912+119insGT
NM_002180.2:c.912+118_912+119insGT , LRG_250t1:c.912+118_912+119insGT NP_002171.2:n.912+118_912+119insGT
XM_005273974.2:c.-100+118_-100+119insGT XP_005274031.1:n.-100+118_-100+119insGT
XM_005273976.1:c.912+118_912+119insGT XP_005274033.1:n.912+118_912+119insGT
XR_247198.1:n.1014+118_1014+119insGT
XR_949903.1:n.1014+118_1014+119insGT
XM_005273976.2:c.912+118_912+119insGT XP_005274033.1:n.912+118_912+119insGT
XM_017017669.2:c.-100+118_-100+119insGT XP_016873158.1:n.-100+118_-100+119insGT
XM_017017670.2:c.-100+118_-100+119insGT XP_016873159.1:n.-100+118_-100+119insGT
XM_017017671.2:c.912+118_912+119insGT XP_016873160.1:n.912+118_912+119insGT
XR_949903.3:n.1010+118_1010+119insGT
NM_002180.3:c.912+118_912+119insGT MANE Select NP_002171.2:n.912+118_912+119insGT