Canonical Allele Identifier: CA381643083

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68675652G>C (hg19) ; chr11:g.68908184G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908184G>C , CM000673.2:g.68908184G>C	GRCh38
NC_000011.9:g.68675652G>C , CM000673.1:g.68675652G>C	GRCh37
NC_000011.8:g.68432228G>C	NCBI36
NG_007976.1:g.9334G>C , LRG_250:g.9334G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.296G>C MANE Select	ENSP00000255078.4:p.Ser99Thr
ENST00000539224.2:c.259G>C
ENST00000674583.1:c.259G>C
ENST00000674597.1:c.107G>C
ENST00000674955.1:c.296G>C	ENSP00000502463.1:p.Ser99Thr
ENST00000675142.1:n.259G>C
ENST00000675469.1:c.172G>C
ENST00000675615.1:c.296G>C	ENSP00000502413.1:p.Ser99Thr
ENST00000675674.1:n.259G>C
ENST00000675873.1:c.259G>C
ENST00000676173.1:n.340G>C
ENST00000676228.1:c.296G>C	ENSP00000502375.1:p.Ser99Thr
ENST00000255078.7:c.296G>C	ENSP00000255078.3:p.Ser99Thr
ENST00000539224.1:c.296G>C	ENSP00000440465.1:p.Ser99Thr
ENST00000544541.1:c.*36G>C	ENSP00000443343.1:n.*36G>C
ENST00000545146.1:c.*166G>C	ENSP00000456366.1:n.*166G>C
NM_002180.2:c.296G>C , LRG_250t1:c.296G>C	NP_002171.2:p.Ser99Thr
XM_005273974.2:c.-716G>C	XP_005274031.1:n.-716G>C
XM_005273976.1:c.296G>C	XP_005274033.1:p.Ser99Thr
XR_247198.1:n.398G>C
XR_949903.1:n.398G>C
XM_005273976.2:c.296G>C	XP_005274033.1:p.Ser99Thr
XM_017017669.2:c.-618G>C	XP_016873158.1:n.-618G>C
XM_017017671.2:c.296G>C	XP_016873160.1:p.Ser99Thr
XR_949903.3:n.394G>C
NM_002180.3:c.296G>C MANE Select	NP_002171.2:p.Ser99Thr