Canonical Allele Identifier: CA381643089

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68908186-C-T
• MyVariant Identifiers: chr11:g.68675654C>T (hg19) ; chr11:g.68908186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908186C>T , CM000673.2:g.68908186C>T	GRCh38
NC_000011.9:g.68675654C>T , CM000673.1:g.68675654C>T	GRCh37
NC_000011.8:g.68432230C>T	NCBI36
NG_007976.1:g.9336C>T , LRG_250:g.9336C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.298C>T MANE Select	ENSP00000255078.4:p.Gln100Ter
ENST00000539224.2:c.261C>T
ENST00000674583.1:c.261C>T
ENST00000674597.1:c.109C>T
ENST00000674955.1:c.298C>T	ENSP00000502463.1:p.Gln100Ter
ENST00000675142.1:n.261C>T
ENST00000675469.1:c.174C>T
ENST00000675615.1:c.298C>T	ENSP00000502413.1:p.Gln100Ter
ENST00000675674.1:n.261C>T
ENST00000675873.1:c.261C>T
ENST00000676173.1:n.342C>T
ENST00000676228.1:c.298C>T	ENSP00000502375.1:p.Gln100Ter
ENST00000255078.7:c.298C>T	ENSP00000255078.3:p.Gln100Ter
ENST00000539224.1:c.298C>T	ENSP00000440465.1:p.Gln100Ter
ENST00000544541.1:c.*38C>T	ENSP00000443343.1:n.*38C>T
ENST00000545146.1:c.*168C>T	ENSP00000456366.1:n.*168C>T
NM_002180.2:c.298C>T , LRG_250t1:c.298C>T	NP_002171.2:p.Gln100Ter
XM_005273974.2:c.-714C>T	XP_005274031.1:n.-714C>T
XM_005273976.1:c.298C>T	XP_005274033.1:p.Gln100Ter
XR_247198.1:n.400C>T
XR_949903.1:n.400C>T
XM_005273976.2:c.298C>T	XP_005274033.1:p.Gln100Ter
XM_017017669.2:c.-616C>T	XP_016873158.1:n.-616C>T
XM_017017671.2:c.298C>T	XP_016873160.1:p.Gln100Ter
XR_949903.3:n.396C>T
NM_002180.3:c.298C>T MANE Select	NP_002171.2:p.Gln100Ter