Canonical Allele Identifier: CA381652637

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs745371869
• MyVariant Identifiers: chr11:g.68703966C>G (hg19) ; chr11:g.68936498C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936498C>G , CM000673.2:g.68936498C>G	GRCh38
NC_000011.9:g.68703966C>G , CM000673.1:g.68703966C>G	GRCh37
NC_000011.8:g.68460542C>G	NCBI36
NG_007976.1:g.37648C>G , LRG_250:g.37648C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2018C>G MANE Select	ENSP00000255078.4:p.Thr673Ser
ENST00000674675.1:c.262C>G
ENST00000674878.1:c.262C>G
ENST00000674955.1:c.*735C>G	ENSP00000502463.1:n.*735C>G
ENST00000675118.1:c.1506C>G
ENST00000675389.1:n.293C>G
ENST00000675615.1:c.2018C>G	ENSP00000502413.1:p.Thr673Ser
ENST00000675648.1:n.1393C>G
ENST00000675916.1:c.262C>G
ENST00000676173.1:n.2763C>G
ENST00000676182.1:c.449C>G
ENST00000676228.1:c.*1341C>G	ENSP00000502375.1:n.*1341C>G
ENST00000255078.7:c.2018C>G	ENSP00000255078.3:p.Thr673Ser
ENST00000539064.5:n.1777C>G
ENST00000543739.5:n.1011C>G
NM_002180.2:c.2018C>G , LRG_250t1:c.2018C>G	NP_002171.2:p.Thr673Ser
XM_005273974.2:c.1007C>G	XP_005274031.1:p.Thr336Ser
XM_005273975.2:c.890C>G	XP_005274032.1:p.Thr297Ser
XM_011544994.1:c.785C>G	XP_011543296.1:p.Thr262Ser
XR_949903.1:n.2120C>G
XM_005273975.3:c.890C>G	XP_005274032.1:p.Thr297Ser
XM_017017669.2:c.1007C>G	XP_016873158.1:p.Thr336Ser
XM_017017670.2:c.1007C>G	XP_016873159.1:p.Thr336Ser
XR_949903.3:n.2116C>G
NM_002180.3:c.2018C>G MANE Select	NP_002171.2:p.Thr673Ser