Canonical Allele Identifier: CA475279662

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704069A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936601A>T , CM000673.2:g.68936601A>T	GRCh38
NC_000011.9:g.68704069A>T , CM000673.1:g.68704069A>T	GRCh37
NC_000011.8:g.68460645A>T	NCBI36
NG_007976.1:g.37751A>T , LRG_250:g.37751A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2121A>T MANE Select	ENSP00000255078.4:p.Pro707=
ENST00000674675.1:c.365A>T
ENST00000674878.1:c.365A>T
ENST00000674955.1:c.*838A>T	ENSP00000502463.1:n.*838A>T
ENST00000675118.1:c.1609A>T
ENST00000675389.1:n.396A>T
ENST00000675615.1:c.2121A>T	ENSP00000502413.1:p.Pro707=
ENST00000675648.1:n.1496A>T
ENST00000675916.1:c.365A>T
ENST00000676173.1:n.2866A>T
ENST00000676182.1:c.552A>T
ENST00000676228.1:c.*1444A>T	ENSP00000502375.1:n.*1444A>T
ENST00000255078.7:c.2121A>T	ENSP00000255078.3:p.Pro707=
ENST00000539064.5:n.1880A>T
ENST00000543739.5:n.1114A>T
NM_002180.2:c.2121A>T , LRG_250t1:c.2121A>T	NP_002171.2:p.Pro707=
XM_005273974.2:c.1110A>T	XP_005274031.1:p.Pro370=
XM_005273975.2:c.993A>T	XP_005274032.1:p.Pro331=
XM_011544994.1:c.888A>T	XP_011543296.1:p.Pro296=
XR_949903.1:n.2223A>T
XM_005273975.3:c.993A>T	XP_005274032.1:p.Pro331=
XM_017017669.2:c.1110A>T	XP_016873158.1:p.Pro370=
XM_017017670.2:c.1110A>T	XP_016873159.1:p.Pro370=
XR_949903.3:n.2219A>T
NM_002180.3:c.2121A>T MANE Select	NP_002171.2:p.Pro707=