Canonical Allele Identifier: CA381653148

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704205C>A (hg19) ; chr11:g.68936737C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936737C>A , CM000673.2:g.68936737C>A	GRCh38
NC_000011.9:g.68704205C>A , CM000673.1:g.68704205C>A	GRCh37
NC_000011.8:g.68460781C>A	NCBI36
NG_007976.1:g.37887C>A , LRG_250:g.37887C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2257C>A MANE Select	ENSP00000255078.4:p.His753Asn
ENST00000674675.1:c.501C>A
ENST00000674878.1:c.501C>A
ENST00000674955.1:c.*974C>A	ENSP00000502463.1:n.*974C>A
ENST00000675118.1:c.1745C>A
ENST00000675389.1:n.532C>A
ENST00000675615.1:c.2257C>A	ENSP00000502413.1:p.His753Asn
ENST00000675648.1:n.1632C>A
ENST00000675916.1:c.501C>A
ENST00000676173.1:n.3002C>A
ENST00000676182.1:c.688C>A
ENST00000676228.1:c.*1580C>A	ENSP00000502375.1:n.*1580C>A
ENST00000255078.7:c.2257C>A	ENSP00000255078.3:p.His753Asn
ENST00000539064.5:n.2016C>A
ENST00000543739.5:n.1250C>A
NM_002180.2:c.2257C>A , LRG_250t1:c.2257C>A	NP_002171.2:p.His753Asn
XM_005273974.2:c.1246C>A	XP_005274031.1:p.His416Asn
XM_005273975.2:c.1129C>A	XP_005274032.1:p.His377Asn
XM_011544994.1:c.1024C>A	XP_011543296.1:p.His342Asn
XR_949903.1:n.2359C>A
XM_005273975.3:c.1129C>A	XP_005274032.1:p.His377Asn
XM_017017669.2:c.1246C>A	XP_016873158.1:p.His416Asn
XM_017017670.2:c.1246C>A	XP_016873159.1:p.His416Asn
XR_949903.3:n.2355C>A
NM_002180.3:c.2257C>A MANE Select	NP_002171.2:p.His753Asn