Canonical Allele Identifier: CA475192290

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68682323G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914855G>C , CM000673.2:g.68914855G>C	GRCh38
NC_000011.9:g.68682323G>C , CM000673.1:g.68682323G>C	GRCh37
NC_000011.8:g.68438899G>C	NCBI36
NG_007976.1:g.16005G>C , LRG_250:g.16005G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.744G>C MANE Select	ENSP00000255078.4:p.Val248=
ENST00000539224.2:c.873G>C
ENST00000674955.1:c.744G>C	ENSP00000502463.1:p.Val248=
ENST00000675118.1:c.91G>C
ENST00000675119.1:c.33G>C	ENSP00000501861.1:p.Val11=
ENST00000675305.1:c.33G>C	ENSP00000502365.1:p.Val11=
ENST00000675464.1:c.33G>C	ENSP00000502650.1:p.Val11=
ENST00000675615.1:c.744G>C	ENSP00000502413.1:p.Val248=
ENST00000675683.1:c.131G>C
ENST00000676173.1:n.788G>C
ENST00000676228.1:c.*67G>C	ENSP00000502375.1:n.*67G>C
ENST00000676239.1:n.58G>C
ENST00000255078.7:c.744G>C	ENSP00000255078.3:p.Val248=
ENST00000539224.1:c.*67G>C	ENSP00000440465.1:n.*67G>C
NM_002180.2:c.744G>C , LRG_250t1:c.744G>C	NP_002171.2:p.Val248=
XM_005273974.2:c.-268G>C	XP_005274031.1:n.-268G>C
XM_005273976.1:c.744G>C	XP_005274033.1:p.Val248=
XR_247198.1:n.846G>C
XR_949903.1:n.846G>C
XM_005273976.2:c.744G>C	XP_005274033.1:p.Val248=
XM_017017669.2:c.-268G>C	XP_016873158.1:n.-268G>C
XM_017017670.2:c.-268G>C	XP_016873159.1:n.-268G>C
XM_017017671.2:c.744G>C	XP_016873160.1:p.Val248=
XR_949903.3:n.842G>C
NM_002180.3:c.744G>C MANE Select	NP_002171.2:p.Val248=