Canonical Allele Identifier: CA381651960

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703860A>T (hg19) ; chr11:g.68936392A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936392A>T , CM000673.2:g.68936392A>T	GRCh38
NC_000011.9:g.68703860A>T , CM000673.1:g.68703860A>T	GRCh37
NC_000011.8:g.68460436A>T	NCBI36
NG_007976.1:g.37542A>T , LRG_250:g.37542A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1912A>T MANE Select	ENSP00000255078.4:p.Thr638Ser
ENST00000674675.1:c.156A>T
ENST00000674878.1:c.156A>T
ENST00000674955.1:c.*629A>T	ENSP00000502463.1:n.*629A>T
ENST00000675118.1:c.1400A>T
ENST00000675389.1:n.187A>T
ENST00000675615.1:c.1912A>T	ENSP00000502413.1:p.Thr638Ser
ENST00000675648.1:n.1287A>T
ENST00000675916.1:c.156A>T
ENST00000676173.1:n.2657A>T
ENST00000676182.1:c.343A>T
ENST00000676228.1:c.*1235A>T	ENSP00000502375.1:n.*1235A>T
ENST00000255078.7:c.1912A>T	ENSP00000255078.3:p.Thr638Ser
ENST00000539064.5:n.1671A>T
ENST00000543739.5:n.905A>T
ENST00000545475.1:n.508A>T
NM_002180.2:c.1912A>T , LRG_250t1:c.1912A>T	NP_002171.2:p.Thr638Ser
XM_005273974.2:c.901A>T	XP_005274031.1:p.Thr301Ser
XM_005273975.2:c.784A>T	XP_005274032.1:p.Thr262Ser
XM_011544994.1:c.679A>T	XP_011543296.1:p.Thr227Ser
XR_949903.1:n.2014A>T
XM_005273975.3:c.784A>T	XP_005274032.1:p.Thr262Ser
XM_017017669.2:c.901A>T	XP_016873158.1:p.Thr301Ser
XM_017017670.2:c.901A>T	XP_016873159.1:p.Thr301Ser
XR_949903.3:n.2010A>T
NM_002180.3:c.1912A>T MANE Select	NP_002171.2:p.Thr638Ser