Canonical Allele Identifier: CA475201681

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68701341T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68933873T>C , CM000673.2:g.68933873T>C	GRCh38
NC_000011.9:g.68701341T>C , CM000673.1:g.68701341T>C	GRCh37
NC_000011.8:g.68457917T>C	NCBI36
NG_007976.1:g.35023T>C , LRG_250:g.35023T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1497T>C MANE Select	ENSP00000255078.4:p.Phe499=
ENST00000674955.1:c.*214T>C	ENSP00000502463.1:n.*214T>C
ENST00000675118.1:c.985T>C
ENST00000675205.1:n.183+392T>C
ENST00000675615.1:c.1497T>C	ENSP00000502413.1:p.Phe499=
ENST00000675648.1:n.872T>C
ENST00000675997.1:n.113-591T>C
ENST00000676173.1:n.2242T>C
ENST00000676228.1:c.*820T>C	ENSP00000502375.1:n.*820T>C
ENST00000255078.7:c.1497T>C	ENSP00000255078.3:p.Phe499=
ENST00000537458.5:n.614T>C
ENST00000539064.5:n.1256T>C
ENST00000541229.5:n.192T>C
ENST00000543739.5:n.614T>C
NM_002180.2:c.1497T>C , LRG_250t1:c.1497T>C	NP_002171.2:p.Phe499=
XM_005273974.2:c.486T>C	XP_005274031.1:p.Phe162=
XM_005273975.2:c.369T>C	XP_005274032.1:p.Phe123=
XM_011544994.1:c.264T>C	XP_011543296.1:p.Phe88=
XR_949903.1:n.1599T>C
XM_005273975.3:c.369T>C	XP_005274032.1:p.Phe123=
XM_017017669.2:c.486T>C	XP_016873158.1:p.Phe162=
XM_017017670.2:c.486T>C	XP_016873159.1:p.Phe162=
XM_017017671.2:c.1497T>C	XP_016873160.1:p.Phe499=
XR_949903.3:n.1595T>C
NM_002180.3:c.1497T>C MANE Select	NP_002171.2:p.Phe499=