Canonical Allele Identifier: CA381651962

Gene: IGHMBP2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1912A>G MANE Select	ENSP00000255078.4:p.Thr638Ala
ENST00000674675.1:c.156A>G
ENST00000674878.1:c.156A>G
ENST00000674955.1:c.*629A>G	ENSP00000502463.1:n.*629A>G
ENST00000675118.1:c.1400A>G
ENST00000675389.1:n.187A>G
ENST00000675615.1:c.1912A>G	ENSP00000502413.1:p.Thr638Ala
ENST00000675648.1:n.1287A>G
ENST00000675916.1:c.156A>G
ENST00000676173.1:n.2657A>G
ENST00000676182.1:c.343A>G
ENST00000676228.1:c.*1235A>G	ENSP00000502375.1:n.*1235A>G
ENST00000255078.7:c.1912A>G	ENSP00000255078.3:p.Thr638Ala
ENST00000539064.5:n.1671A>G
ENST00000543739.5:n.905A>G
ENST00000545475.1:n.508A>G
NM_002180.2:c.1912A>G , LRG_250t1:c.1912A>G	NP_002171.2:p.Thr638Ala
XM_005273974.2:c.901A>G	XP_005274031.1:p.Thr301Ala
XM_005273975.2:c.784A>G	XP_005274032.1:p.Thr262Ala
XM_011544994.1:c.679A>G	XP_011543296.1:p.Thr227Ala
XR_949903.1:n.2014A>G
XM_005273975.3:c.784A>G	XP_005274032.1:p.Thr262Ala
XM_017017669.2:c.901A>G	XP_016873158.1:p.Thr301Ala
XM_017017670.2:c.901A>G	XP_016873159.1:p.Thr301Ala
XR_949903.3:n.2010A>G
NM_002180.3:c.1912A>G MANE Select	NP_002171.2:p.Thr638Ala