Canonical Allele Identifier: CA475280899

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704399G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936931G>A , CM000673.2:g.68936931G>A	GRCh38
NC_000011.9:g.68704399G>A , CM000673.1:g.68704399G>A	GRCh37
NC_000011.8:g.68460975G>A	NCBI36
NG_007976.1:g.38081G>A , LRG_250:g.38081G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2451G>A MANE Select	ENSP00000255078.4:p.Gln817=
ENST00000674675.1:c.596G>A
ENST00000674878.1:c.556G>A
ENST00000675118.1:c.1939G>A
ENST00000675389.1:n.726G>A
ENST00000675615.1:c.2451G>A	ENSP00000502413.1:p.Gln817=
ENST00000675648.1:n.1826G>A
ENST00000675916.1:c.695G>A
ENST00000676173.1:n.3196G>A
ENST00000676182.1:c.882G>A
ENST00000676228.1:c.*1774G>A	ENSP00000502375.1:n.*1774G>A
ENST00000255078.7:c.2451G>A	ENSP00000255078.3:p.Gln817=
ENST00000539064.5:n.2210G>A
ENST00000543739.5:n.1444G>A
NM_002180.2:c.2451G>A , LRG_250t1:c.2451G>A	NP_002171.2:p.Gln817=
XM_005273974.2:c.1440G>A	XP_005274031.1:p.Gln480=
XM_005273975.2:c.1323G>A	XP_005274032.1:p.Gln441=
XM_011544994.1:c.1218G>A	XP_011543296.1:p.Gln406=
XR_949903.1:n.2553G>A
XM_005273975.3:c.1323G>A	XP_005274032.1:p.Gln441=
XM_017017669.2:c.1440G>A	XP_016873158.1:p.Gln480=
XM_017017670.2:c.1440G>A	XP_016873159.1:p.Gln480=
XR_949903.3:n.2549G>A
NM_002180.3:c.2451G>A MANE Select	NP_002171.2:p.Gln817=