Canonical Allele Identifier: CA381643446

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68676019A>G (hg19) ; chr11:g.68908551A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908551A>G , CM000673.2:g.68908551A>G	GRCh38
NC_000011.9:g.68676019A>G , CM000673.1:g.68676019A>G	GRCh37
NC_000011.8:g.68432595A>G	NCBI36
NG_007976.1:g.9701A>G , LRG_250:g.9701A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.467A>G MANE Select	ENSP00000255078.4:p.Lys156Arg
ENST00000539224.2:c.430A>G
ENST00000674583.1:c.430A>G
ENST00000674597.1:c.278A>G
ENST00000674955.1:c.467A>G	ENSP00000502463.1:p.Lys156Arg
ENST00000675142.1:n.430A>G
ENST00000675469.1:c.343A>G
ENST00000675615.1:c.467A>G	ENSP00000502413.1:p.Lys156Arg
ENST00000675674.1:n.430A>G
ENST00000675683.1:c.18A>G
ENST00000675873.1:c.430A>G
ENST00000676173.1:n.511A>G
ENST00000676228.1:c.449+214A>G	ENSP00000502375.1:n.449+214A>G
ENST00000255078.7:c.467A>G	ENSP00000255078.3:p.Lys156Arg
ENST00000539224.1:c.449+214A>G	ENSP00000440465.1:n.449+214A>G
ENST00000544541.1:c.*207A>G	ENSP00000443343.1:n.*207A>G
NM_002180.2:c.467A>G , LRG_250t1:c.467A>G	NP_002171.2:p.Lys156Arg
XM_005273974.2:c.-545A>G	XP_005274031.1:n.-545A>G
XM_005273976.1:c.467A>G	XP_005274033.1:p.Lys156Arg
XR_247198.1:n.569A>G
XR_949903.1:n.569A>G
XM_005273976.2:c.467A>G	XP_005274033.1:p.Lys156Arg
XM_017017669.2:c.-465+214A>G	XP_016873158.1:n.-465+214A>G
XM_017017671.2:c.467A>G	XP_016873160.1:p.Lys156Arg
XR_949903.3:n.565A>G
NM_002180.3:c.467A>G MANE Select	NP_002171.2:p.Lys156Arg