Canonical Allele Identifier: CA475187593

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68676011T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908543T>C , CM000673.2:g.68908543T>C	GRCh38
NC_000011.9:g.68676011T>C , CM000673.1:g.68676011T>C	GRCh37
NC_000011.8:g.68432587T>C	NCBI36
NG_007976.1:g.9693T>C , LRG_250:g.9693T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.459T>C MANE Select	ENSP00000255078.4:p.Ile153=
ENST00000539224.2:c.422T>C
ENST00000674583.1:c.422T>C
ENST00000674597.1:c.270T>C
ENST00000674955.1:c.459T>C	ENSP00000502463.1:p.Ile153=
ENST00000675142.1:n.422T>C
ENST00000675469.1:c.335T>C
ENST00000675615.1:c.459T>C	ENSP00000502413.1:p.Ile153=
ENST00000675674.1:n.422T>C
ENST00000675683.1:c.10T>C
ENST00000675873.1:c.422T>C
ENST00000676173.1:n.503T>C
ENST00000676228.1:c.449+206T>C	ENSP00000502375.1:n.449+206T>C
ENST00000255078.7:c.459T>C	ENSP00000255078.3:p.Ile153=
ENST00000539224.1:c.449+206T>C	ENSP00000440465.1:n.449+206T>C
ENST00000544541.1:c.*199T>C	ENSP00000443343.1:n.*199T>C
NM_002180.2:c.459T>C , LRG_250t1:c.459T>C	NP_002171.2:p.Ile153=
XM_005273974.2:c.-553T>C	XP_005274031.1:n.-553T>C
XM_005273976.1:c.459T>C	XP_005274033.1:p.Ile153=
XR_247198.1:n.561T>C
XR_949903.1:n.561T>C
XM_005273976.2:c.459T>C	XP_005274033.1:p.Ile153=
XM_017017669.2:c.-465+206T>C	XP_016873158.1:n.-465+206T>C
XM_017017671.2:c.459T>C	XP_016873160.1:p.Ile153=
XR_949903.3:n.557T>C
NM_002180.3:c.459T>C MANE Select	NP_002171.2:p.Ile153=