Canonical Allele Identifier: CA475193269
Gene: IGHMBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.68682404T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68914936T>A , CM000673.2:g.68914936T>A GRCh38
NC_000011.9:g.68682404T>A , CM000673.1:g.68682404T>A GRCh37
NC_000011.8:g.68438980T>A NCBI36
NG_007976.1:g.16086T>A , LRG_250:g.16086T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.825T>A MANE Select ENSP00000255078.4:p.Ile275=
ENST00000539224.2:c.954T>A
ENST00000674955.1:c.825T>A ENSP00000502463.1:p.Ile275=
ENST00000675118.1:c.172T>A
ENST00000675119.1:c.114T>A ENSP00000501861.1:p.Ile38=
ENST00000675305.1:c.114T>A ENSP00000502365.1:p.Ile38=
ENST00000675464.1:c.114T>A ENSP00000502650.1:p.Ile38=
ENST00000675615.1:c.825T>A ENSP00000502413.1:p.Ile275=
ENST00000675683.1:c.212T>A
ENST00000676173.1:n.869T>A
ENST00000676228.1:c.*148T>A ENSP00000502375.1:n.*148T>A
ENST00000676239.1:n.139T>A
ENST00000255078.7:c.825T>A ENSP00000255078.3:p.Ile275=
ENST00000539224.1:c.*148T>A ENSP00000440465.1:n.*148T>A
NM_002180.2:c.825T>A , LRG_250t1:c.825T>A NP_002171.2:p.Ile275=
XM_005273974.2:c.-187T>A XP_005274031.1:n.-187T>A
XM_005273976.1:c.825T>A XP_005274033.1:p.Ile275=
XR_247198.1:n.927T>A
XR_949903.1:n.927T>A
XM_005273976.2:c.825T>A XP_005274033.1:p.Ile275=
XM_017017669.2:c.-187T>A XP_016873158.1:n.-187T>A
XM_017017670.2:c.-187T>A XP_016873159.1:n.-187T>A
XM_017017671.2:c.825T>A XP_016873160.1:p.Ile275=
XR_949903.3:n.923T>A
NM_002180.3:c.825T>A MANE Select NP_002171.2:p.Ile275=