Canonical Allele Identifier: CA381643407

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68676000A>C (hg19) ; chr11:g.68908532A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908532A>C , CM000673.2:g.68908532A>C	GRCh38
NC_000011.9:g.68676000A>C , CM000673.1:g.68676000A>C	GRCh37
NC_000011.8:g.68432576A>C	NCBI36
NG_007976.1:g.9682A>C , LRG_250:g.9682A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.450-2A>C MANE Select	ENSP00000255078.4:n.450-2A>C
ENST00000539224.2:c.413-2A>C
ENST00000674583.1:c.413-2A>C
ENST00000674597.1:c.261-2A>C
ENST00000674955.1:c.450-2A>C	ENSP00000502463.1:n.450-2A>C
ENST00000675142.1:n.413-2A>C
ENST00000675469.1:c.326-2A>C
ENST00000675615.1:c.450-2A>C	ENSP00000502413.1:n.450-2A>C
ENST00000675674.1:n.413-2A>C
ENST00000675873.1:c.413-2A>C
ENST00000676173.1:n.494-2A>C
ENST00000676228.1:c.449+195A>C	ENSP00000502375.1:n.449+195A>C
ENST00000255078.7:c.450-2A>C	ENSP00000255078.3:n.450-2A>C
ENST00000539224.1:c.449+195A>C	ENSP00000440465.1:n.449+195A>C
ENST00000544541.1:c.*190-2A>C	ENSP00000443343.1:n.*190-2A>C
NM_002180.2:c.450-2A>C , LRG_250t1:c.450-2A>C	NP_002171.2:n.450-2A>C
XM_005273974.2:c.-562-2A>C	XP_005274031.1:n.-562-2A>C
XM_005273976.1:c.450-2A>C	XP_005274033.1:n.450-2A>C
XR_247198.1:n.552-2A>C
XR_949903.1:n.552-2A>C
XM_005273976.2:c.450-2A>C	XP_005274033.1:n.450-2A>C
XM_017017669.2:c.-465+195A>C	XP_016873158.1:n.-465+195A>C
XM_017017671.2:c.450-2A>C	XP_016873160.1:n.450-2A>C
XR_949903.3:n.548-2A>C
NM_002180.3:c.450-2A>C MANE Select	NP_002171.2:n.450-2A>C