Canonical Allele Identifier: CA381651644

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703773G>T (hg19) ; chr11:g.68936305G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936305G>T , CM000673.2:g.68936305G>T	GRCh38
NC_000011.9:g.68703773G>T , CM000673.1:g.68703773G>T	GRCh37
NC_000011.8:g.68460349G>T	NCBI36
NG_007976.1:g.37455G>T , LRG_250:g.37455G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1825G>T MANE Select	ENSP00000255078.4:p.Ala609Ser
ENST00000674675.1:c.69G>T
ENST00000674878.1:c.69G>T
ENST00000674955.1:c.*542G>T	ENSP00000502463.1:n.*542G>T
ENST00000675118.1:c.1313G>T
ENST00000675389.1:n.100G>T
ENST00000675615.1:c.1825G>T	ENSP00000502413.1:p.Ala609Ser
ENST00000675648.1:n.1200G>T
ENST00000675916.1:c.69G>T
ENST00000676173.1:n.2570G>T
ENST00000676182.1:c.256G>T
ENST00000676228.1:c.*1148G>T	ENSP00000502375.1:n.*1148G>T
ENST00000255078.7:c.1825G>T	ENSP00000255078.3:p.Ala609Ser
ENST00000539064.5:n.1584G>T
ENST00000541229.5:n.520G>T
ENST00000543739.5:n.818G>T
ENST00000545475.1:n.421G>T
NM_002180.2:c.1825G>T , LRG_250t1:c.1825G>T	NP_002171.2:p.Ala609Ser
XM_005273974.2:c.814G>T	XP_005274031.1:p.Ala272Ser
XM_005273975.2:c.697G>T	XP_005274032.1:p.Ala233Ser
XM_011544994.1:c.592G>T	XP_011543296.1:p.Ala198Ser
XR_949903.1:n.1927G>T
XM_005273975.3:c.697G>T	XP_005274032.1:p.Ala233Ser
XM_017017669.2:c.814G>T	XP_016873158.1:p.Ala272Ser
XM_017017670.2:c.814G>T	XP_016873159.1:p.Ala272Ser
XR_949903.3:n.1923G>T
NM_002180.3:c.1825G>T MANE Select	NP_002171.2:p.Ala609Ser