Canonical Allele Identifier: CA381643192

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68675709T>A (hg19) ; chr11:g.68908241T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908241T>A , CM000673.2:g.68908241T>A	GRCh38
NC_000011.9:g.68675709T>A , CM000673.1:g.68675709T>A	GRCh37
NC_000011.8:g.68432285T>A	NCBI36
NG_007976.1:g.9391T>A , LRG_250:g.9391T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.353T>A MANE Select	ENSP00000255078.4:p.Phe118Tyr
ENST00000539224.2:c.316T>A
ENST00000674583.1:c.316T>A
ENST00000674597.1:c.164T>A
ENST00000674955.1:c.353T>A	ENSP00000502463.1:p.Phe118Tyr
ENST00000675142.1:n.316T>A
ENST00000675469.1:c.229T>A
ENST00000675615.1:c.353T>A	ENSP00000502413.1:p.Phe118Tyr
ENST00000675674.1:n.316T>A
ENST00000675873.1:c.316T>A
ENST00000676173.1:n.397T>A
ENST00000676228.1:c.353T>A	ENSP00000502375.1:p.Phe118Tyr
ENST00000255078.7:c.353T>A	ENSP00000255078.3:p.Phe118Tyr
ENST00000539224.1:c.353T>A	ENSP00000440465.1:p.Phe118Tyr
ENST00000544541.1:c.*93T>A	ENSP00000443343.1:n.*93T>A
NM_002180.2:c.353T>A , LRG_250t1:c.353T>A	NP_002171.2:p.Phe118Tyr
XM_005273974.2:c.-659T>A	XP_005274031.1:n.-659T>A
XM_005273976.1:c.353T>A	XP_005274033.1:p.Phe118Tyr
XR_247198.1:n.455T>A
XR_949903.1:n.455T>A
XM_005273976.2:c.353T>A	XP_005274033.1:p.Phe118Tyr
XM_017017669.2:c.-561T>A	XP_016873158.1:n.-561T>A
XM_017017671.2:c.353T>A	XP_016873160.1:p.Phe118Tyr
XR_949903.3:n.451T>A
NM_002180.3:c.353T>A MANE Select	NP_002171.2:p.Phe118Tyr