Canonical Allele Identifier: CA381653125

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704194C>A (hg19) ; chr11:g.68936726C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936726C>A , CM000673.2:g.68936726C>A	GRCh38
NC_000011.9:g.68704194C>A , CM000673.1:g.68704194C>A	GRCh37
NC_000011.8:g.68460770C>A	NCBI36
NG_007976.1:g.37876C>A , LRG_250:g.37876C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2246C>A MANE Select	ENSP00000255078.4:p.Ser749Tyr
ENST00000674675.1:c.490C>A
ENST00000674878.1:c.490C>A
ENST00000674955.1:c.*963C>A	ENSP00000502463.1:n.*963C>A
ENST00000675118.1:c.1734C>A
ENST00000675389.1:n.521C>A
ENST00000675615.1:c.2246C>A	ENSP00000502413.1:p.Ser749Tyr
ENST00000675648.1:n.1621C>A
ENST00000675916.1:c.490C>A
ENST00000676173.1:n.2991C>A
ENST00000676182.1:c.677C>A
ENST00000676228.1:c.*1569C>A	ENSP00000502375.1:n.*1569C>A
ENST00000255078.7:c.2246C>A	ENSP00000255078.3:p.Ser749Tyr
ENST00000539064.5:n.2005C>A
ENST00000543739.5:n.1239C>A
NM_002180.2:c.2246C>A , LRG_250t1:c.2246C>A	NP_002171.2:p.Ser749Tyr
XM_005273974.2:c.1235C>A	XP_005274031.1:p.Ser412Tyr
XM_005273975.2:c.1118C>A	XP_005274032.1:p.Ser373Tyr
XM_011544994.1:c.1013C>A	XP_011543296.1:p.Ser338Tyr
XR_949903.1:n.2348C>A
XM_005273975.3:c.1118C>A	XP_005274032.1:p.Ser373Tyr
XM_017017669.2:c.1235C>A	XP_016873158.1:p.Ser412Tyr
XM_017017670.2:c.1235C>A	XP_016873159.1:p.Ser412Tyr
XR_949903.3:n.2344C>A
NM_002180.3:c.2246C>A MANE Select	NP_002171.2:p.Ser749Tyr