Canonical Allele Identifier: CA2792557351
Gene: IGHMBP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68915196_68915197insTTTTAAATTTTTTTTTTTTTTTTTTT , CM000673.2:g.68915196_68915197insTTTTAAATTTTTTTTTTTTTTTTTTT GRCh38
NC_000011.9:g.68682664_68682665insTTTTAAATTTTTTTTTTTTTTTTTTT , CM000673.1:g.68682664_68682665insTTTTAAATTTTTTTTTTTTTTTTTTT GRCh37
NC_000011.8:g.68439240_68439241insTTTTAAATTTTTTTTTTTTTTTTTTT NCBI36
NG_007976.1:g.16346_16347insTTTTAAATTTTTTTTTTTTTTTTTTT , LRG_250:g.16346_16347insTTTTAAATTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT MANE Select ENSP00000255078.4:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTT...
ENST00000539224.2:c.1041+173_1041+174insTTTTAAATTTTTTTTTTTTTTTTTTT
ENST00000674955.1:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT ENSP00000502463.1:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTT...
ENST00000675118.1:c.259+173_259+174insTTTTAAATTTTTTTTTTTTTTTTTTT
ENST00000675119.1:c.201+173_201+174insTTTTAAATTTTTTTTTTTTTTTTTTT ENSP00000501861.1:n.201+173_201+174insTTTTAAATTTTTTTTTTTTTTTT...
ENST00000675305.1:c.201+173_201+174insTTTTAAATTTTTTTTTTTTTTTTTTT ENSP00000502365.1:n.201+173_201+174insTTTTAAATTTTTTTTTTTTTTTT...
ENST00000675464.1:c.195+179_195+180insTTTTAAATTTTTTTTTTTTTTTTTTT ENSP00000502650.1:n.195+179_195+180insTTTTAAATTTTTTTTTTTTTTTT...
ENST00000675615.1:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT ENSP00000502413.1:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTT...
ENST00000675683.1:c.299+173_299+174insTTTTAAATTTTTTTTTTTTTTTTTTT
ENST00000676173.1:n.956+173_956+174insTTTTAAATTTTTTTTTTTTTTTTTTT
ENST00000676228.1:c.*235+173_*235+174insTTTTAAATTTTTTTTTTTTTTTTTTT ENSP00000502375.1:n.*235+173_*235+174insTTTTAAATTTTTTTTTTTTTT...
ENST00000255078.7:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT ENSP00000255078.3:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTT...
NM_002180.2:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT , LRG_250t1:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT NP_002171.2:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT
XM_005273974.2:c.-100+173_-100+174insTTTTAAATTTTTTTTTTTTTTTTTTT XP_005274031.1:n.-100+173_-100+174insTTTTAAATTTTTTTTTTTTTTTTT...
XM_005273976.1:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT XP_005274033.1:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT...
XR_247198.1:n.1014+173_1014+174insTTTTAAATTTTTTTTTTTTTTTTTTT
XR_949903.1:n.1014+173_1014+174insTTTTAAATTTTTTTTTTTTTTTTTTT
XM_005273976.2:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT XP_005274033.1:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT...
XM_017017669.2:c.-100+173_-100+174insTTTTAAATTTTTTTTTTTTTTTTTTT XP_016873158.1:n.-100+173_-100+174insTTTTAAATTTTTTTTTTTTTTTTT...
XM_017017670.2:c.-100+173_-100+174insTTTTAAATTTTTTTTTTTTTTTTTTT XP_016873159.1:n.-100+173_-100+174insTTTTAAATTTTTTTTTTTTTTTTT...
XM_017017671.2:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT XP_016873160.1:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT...
XR_949903.3:n.1010+173_1010+174insTTTTAAATTTTTTTTTTTTTTTTTTT
NM_002180.3:c.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT MANE Select NP_002171.2:n.912+173_912+174insTTTTAAATTTTTTTTTTTTTTTTTTT