Canonical Allele Identifier: CA475204539
Gene: IGHMBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.68704460C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68936992C>T , CM000673.2:g.68936992C>T GRCh38
NC_000011.9:g.68704460C>T , CM000673.1:g.68704460C>T GRCh37
NC_000011.8:g.68461036C>T NCBI36
NG_007976.1:g.38142C>T , LRG_250:g.38142C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.2512C>T MANE Select ENSP00000255078.4:p.Leu838=
ENST00000674675.1:c.657C>T
ENST00000674878.1:c.617C>T
ENST00000675118.1:c.2000C>T
ENST00000675389.1:n.787C>T
ENST00000675615.1:c.2512C>T ENSP00000502413.1:p.Leu838=
ENST00000675648.1:n.1887C>T
ENST00000675916.1:c.756C>T
ENST00000676173.1:n.3257C>T
ENST00000676182.1:c.943C>T
ENST00000676228.1:c.*1835C>T ENSP00000502375.1:n.*1835C>T
ENST00000255078.7:c.2512C>T ENSP00000255078.3:p.Leu838=
ENST00000539064.5:n.2271C>T
ENST00000543739.5:n.1505C>T
NM_002180.2:c.2512C>T , LRG_250t1:c.2512C>T NP_002171.2:p.Leu838=
XM_005273974.2:c.1501C>T XP_005274031.1:p.Leu501=
XM_005273975.2:c.1384C>T XP_005274032.1:p.Leu462=
XM_011544994.1:c.1279C>T XP_011543296.1:p.Leu427=
XR_949903.1:n.2614C>T
XM_005273975.3:c.1384C>T XP_005274032.1:p.Leu462=
XM_017017669.2:c.1501C>T XP_016873158.1:p.Leu501=
XM_017017670.2:c.1501C>T XP_016873159.1:p.Leu501=
XR_949903.3:n.2610C>T
NM_002180.3:c.2512C>T MANE Select NP_002171.2:p.Leu838=