Canonical Allele Identifier: CA381652872

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704080G>T (hg19) ; chr11:g.68936612G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936612G>T , CM000673.2:g.68936612G>T	GRCh38
NC_000011.9:g.68704080G>T , CM000673.1:g.68704080G>T	GRCh37
NC_000011.8:g.68460656G>T	NCBI36
NG_007976.1:g.37762G>T , LRG_250:g.37762G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2132G>T MANE Select	ENSP00000255078.4:p.Ser711Ile
ENST00000674675.1:c.376G>T
ENST00000674878.1:c.376G>T
ENST00000674955.1:c.*849G>T	ENSP00000502463.1:n.*849G>T
ENST00000675118.1:c.1620G>T
ENST00000675389.1:n.407G>T
ENST00000675615.1:c.2132G>T	ENSP00000502413.1:p.Ser711Ile
ENST00000675648.1:n.1507G>T
ENST00000675916.1:c.376G>T
ENST00000676173.1:n.2877G>T
ENST00000676182.1:c.563G>T
ENST00000676228.1:c.*1455G>T	ENSP00000502375.1:n.*1455G>T
ENST00000255078.7:c.2132G>T	ENSP00000255078.3:p.Ser711Ile
ENST00000539064.5:n.1891G>T
ENST00000543739.5:n.1125G>T
NM_002180.2:c.2132G>T , LRG_250t1:c.2132G>T	NP_002171.2:p.Ser711Ile
XM_005273974.2:c.1121G>T	XP_005274031.1:p.Ser374Ile
XM_005273975.2:c.1004G>T	XP_005274032.1:p.Ser335Ile
XM_011544994.1:c.899G>T	XP_011543296.1:p.Ser300Ile
XR_949903.1:n.2234G>T
XM_005273975.3:c.1004G>T	XP_005274032.1:p.Ser335Ile
XM_017017669.2:c.1121G>T	XP_016873158.1:p.Ser374Ile
XM_017017670.2:c.1121G>T	XP_016873159.1:p.Ser374Ile
XR_949903.3:n.2230G>T
NM_002180.3:c.2132G>T MANE Select	NP_002171.2:p.Ser711Ile