Canonical Allele Identifier: CA6153199
Gene: IGHMBP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68906133C>G , CM000673.2:g.68906133C>G GRCh38
NC_000011.9:g.68673601C>G , CM000673.1:g.68673601C>G GRCh37
NC_000011.8:g.68430177C>G NCBI36
NG_007976.1:g.7283C>G , LRG_250:g.7283C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.151C>G MANE Select ENSP00000255078.4:p.Gln51Glu
ENST00000539224.2:c.114C>G
ENST00000674583.1:c.114C>G
ENST00000674597.1:c.65C>G
ENST00000674729.1:n.94C>G
ENST00000674955.1:c.151C>G ENSP00000502463.1:p.Gln51Glu
ENST00000675142.1:n.114C>G
ENST00000675469.1:c.65C>G
ENST00000675615.1:c.151C>G ENSP00000502413.1:p.Gln51Glu
ENST00000675674.1:n.114C>G
ENST00000675800.1:n.96C>G
ENST00000675873.1:c.114C>G
ENST00000676173.1:n.191C>G
ENST00000676228.1:c.151C>G ENSP00000502375.1:p.Gln51Glu
ENST00000255078.7:c.151C>G ENSP00000255078.3:p.Gln51Glu
ENST00000539224.1:c.151C>G ENSP00000440465.1:p.Gln51Glu
ENST00000544541.1:c.87-2012C>G ENSP00000443343.1:n.87-2012C>G
ENST00000545146.1:c.151C>G ENSP00000456366.1:p.Gln51Glu
NM_002180.2:c.151C>G , LRG_250t1:c.151C>G NP_002171.2:p.Gln51Glu
XM_005273974.2:c.-865C>G XP_005274031.1:n.-865C>G
XM_005273976.1:c.151C>G XP_005274033.1:p.Gln51Glu
XR_247198.1:n.253C>G
XR_949903.1:n.253C>G
XM_005273976.2:c.151C>G XP_005274033.1:p.Gln51Glu
XM_017017669.2:c.-763C>G XP_016873158.1:n.-763C>G
XM_017017671.2:c.151C>G XP_016873160.1:p.Gln51Glu
XR_949903.3:n.249C>G
NM_002180.3:c.151C>G MANE Select NP_002171.2:p.Gln51Glu