Canonical Allele Identifier: CA381643092

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68675655A>C (hg19) ; chr11:g.68908187A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908187A>C , CM000673.2:g.68908187A>C	GRCh38
NC_000011.9:g.68675655A>C , CM000673.1:g.68675655A>C	GRCh37
NC_000011.8:g.68432231A>C	NCBI36
NG_007976.1:g.9337A>C , LRG_250:g.9337A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.299A>C MANE Select	ENSP00000255078.4:p.Gln100Pro
ENST00000539224.2:c.262A>C
ENST00000674583.1:c.262A>C
ENST00000674597.1:c.110A>C
ENST00000674955.1:c.299A>C	ENSP00000502463.1:p.Gln100Pro
ENST00000675142.1:n.262A>C
ENST00000675469.1:c.175A>C
ENST00000675615.1:c.299A>C	ENSP00000502413.1:p.Gln100Pro
ENST00000675674.1:n.262A>C
ENST00000675873.1:c.262A>C
ENST00000676173.1:n.343A>C
ENST00000676228.1:c.299A>C	ENSP00000502375.1:p.Gln100Pro
ENST00000255078.7:c.299A>C	ENSP00000255078.3:p.Gln100Pro
ENST00000539224.1:c.299A>C	ENSP00000440465.1:p.Gln100Pro
ENST00000544541.1:c.*39A>C	ENSP00000443343.1:n.*39A>C
ENST00000545146.1:c.*169A>C	ENSP00000456366.1:n.*169A>C
NM_002180.2:c.299A>C , LRG_250t1:c.299A>C	NP_002171.2:p.Gln100Pro
XM_005273974.2:c.-713A>C	XP_005274031.1:n.-713A>C
XM_005273976.1:c.299A>C	XP_005274033.1:p.Gln100Pro
XR_247198.1:n.401A>C
XR_949903.1:n.401A>C
XM_005273976.2:c.299A>C	XP_005274033.1:p.Gln100Pro
XM_017017669.2:c.-615A>C	XP_016873158.1:n.-615A>C
XM_017017671.2:c.299A>C	XP_016873160.1:p.Gln100Pro
XR_949903.3:n.397A>C
NM_002180.3:c.299A>C MANE Select	NP_002171.2:p.Gln100Pro