Canonical Allele Identifier: CA381643134

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68908210-C-G
• MyVariant Identifiers: chr11:g.68675678C>G (hg19) ; chr11:g.68908210C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908210C>G , CM000673.2:g.68908210C>G	GRCh38
NC_000011.9:g.68675678C>G , CM000673.1:g.68675678C>G	GRCh37
NC_000011.8:g.68432254C>G	NCBI36
NG_007976.1:g.9360C>G , LRG_250:g.9360C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.322C>G MANE Select	ENSP00000255078.4:p.Arg108Gly
ENST00000539224.2:c.285C>G
ENST00000674583.1:c.285C>G
ENST00000674597.1:c.133C>G
ENST00000674955.1:c.322C>G	ENSP00000502463.1:p.Arg108Gly
ENST00000675142.1:n.285C>G
ENST00000675469.1:c.198C>G
ENST00000675615.1:c.322C>G	ENSP00000502413.1:p.Arg108Gly
ENST00000675674.1:n.285C>G
ENST00000675873.1:c.285C>G
ENST00000676173.1:n.366C>G
ENST00000676228.1:c.322C>G	ENSP00000502375.1:p.Arg108Gly
ENST00000255078.7:c.322C>G	ENSP00000255078.3:p.Arg108Gly
ENST00000539224.1:c.322C>G	ENSP00000440465.1:p.Arg108Gly
ENST00000544541.1:c.*62C>G	ENSP00000443343.1:n.*62C>G
NM_002180.2:c.322C>G , LRG_250t1:c.322C>G	NP_002171.2:p.Arg108Gly
XM_005273974.2:c.-690C>G	XP_005274031.1:n.-690C>G
XM_005273976.1:c.322C>G	XP_005274033.1:p.Arg108Gly
XR_247198.1:n.424C>G
XR_949903.1:n.424C>G
XM_005273976.2:c.322C>G	XP_005274033.1:p.Arg108Gly
XM_017017669.2:c.-592C>G	XP_016873158.1:n.-592C>G
XM_017017671.2:c.322C>G	XP_016873160.1:p.Arg108Gly
XR_949903.3:n.420C>G
NM_002180.3:c.322C>G MANE Select	NP_002171.2:p.Arg108Gly