Canonical Allele Identifier: CA475194804
Gene: IGHMBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.68685251A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68917783A>G , CM000673.2:g.68917783A>G GRCh38
NC_000011.9:g.68685251A>G , CM000673.1:g.68685251A>G GRCh37
NC_000011.8:g.68441827A>G NCBI36
NG_007976.1:g.18933A>G , LRG_250:g.18933A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.960A>G MANE Select ENSP00000255078.4:p.Arg320=
ENST00000674745.1:c.48A>G ENSP00000502738.1:p.Arg16=
ENST00000674775.1:n.48A>G
ENST00000674955.1:c.960A>G ENSP00000502463.1:p.Arg320=
ENST00000675118.1:c.448A>G
ENST00000675119.1:c.387A>G ENSP00000501861.1:n.387A>G
ENST00000675305.1:c.280A>G ENSP00000502365.1:n.280A>G
ENST00000675464.1:c.243A>G ENSP00000502650.1:p.Arg81=
ENST00000675493.1:n.48A>G
ENST00000675615.1:c.960A>G ENSP00000502413.1:p.Arg320=
ENST00000675648.1:n.335A>G
ENST00000675683.1:c.347A>G
ENST00000675684.1:c.48A>G ENSP00000502192.1:p.Arg16=
ENST00000676173.1:n.1004A>G
ENST00000676228.1:c.*283A>G ENSP00000502375.1:n.*283A>G
ENST00000255078.7:c.960A>G ENSP00000255078.3:p.Arg320=
NM_002180.2:c.960A>G , LRG_250t1:c.960A>G NP_002171.2:p.Arg320=
XM_005273974.2:c.-52A>G XP_005274031.1:n.-52A>G
XM_005273976.1:c.960A>G XP_005274033.1:p.Arg320=
XR_247198.1:n.1062A>G
XR_949903.1:n.1062A>G
XM_005273976.2:c.960A>G XP_005274033.1:p.Arg320=
XM_017017669.2:c.-52A>G XP_016873158.1:n.-52A>G
XM_017017670.2:c.-52A>G XP_016873159.1:n.-52A>G
XM_017017671.2:c.960A>G XP_016873160.1:p.Arg320=
XR_949903.3:n.1058A>G
NM_002180.3:c.960A>G MANE Select NP_002171.2:p.Arg320=