Canonical Allele Identifier: CA475279471

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704042T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936574T>G , CM000673.2:g.68936574T>G	GRCh38
NC_000011.9:g.68704042T>G , CM000673.1:g.68704042T>G	GRCh37
NC_000011.8:g.68460618T>G	NCBI36
NG_007976.1:g.37724T>G , LRG_250:g.37724T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2094T>G MANE Select	ENSP00000255078.4:p.Ala698=
ENST00000674675.1:c.338T>G
ENST00000674878.1:c.338T>G
ENST00000674955.1:c.*811T>G	ENSP00000502463.1:n.*811T>G
ENST00000675118.1:c.1582T>G
ENST00000675389.1:n.369T>G
ENST00000675615.1:c.2094T>G	ENSP00000502413.1:p.Ala698=
ENST00000675648.1:n.1469T>G
ENST00000675916.1:c.338T>G
ENST00000676173.1:n.2839T>G
ENST00000676182.1:c.525T>G
ENST00000676228.1:c.*1417T>G	ENSP00000502375.1:n.*1417T>G
ENST00000255078.7:c.2094T>G	ENSP00000255078.3:p.Ala698=
ENST00000539064.5:n.1853T>G
ENST00000543739.5:n.1087T>G
NM_002180.2:c.2094T>G , LRG_250t1:c.2094T>G	NP_002171.2:p.Ala698=
XM_005273974.2:c.1083T>G	XP_005274031.1:p.Ala361=
XM_005273975.2:c.966T>G	XP_005274032.1:p.Ala322=
XM_011544994.1:c.861T>G	XP_011543296.1:p.Ala287=
XR_949903.1:n.2196T>G
XM_005273975.3:c.966T>G	XP_005274032.1:p.Ala322=
XM_017017669.2:c.1083T>G	XP_016873158.1:p.Ala361=
XM_017017670.2:c.1083T>G	XP_016873159.1:p.Ala361=
XR_949903.3:n.2192T>G
NM_002180.3:c.2094T>G MANE Select	NP_002171.2:p.Ala698=