Canonical Allele Identifier: CA6153542

Gene: IGHMBP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68929320G>A , CM000673.2:g.68929320G>A	GRCh38
NC_000011.9:g.68696788G>A , CM000673.1:g.68696788G>A	GRCh37
NC_000011.8:g.68453364G>A	NCBI36
NG_007976.1:g.30470G>A , LRG_250:g.30470G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1198G>A MANE Select	ENSP00000255078.4:p.Asp400Asn
ENST00000674698.1:n.138G>A
ENST00000674745.1:c.363G>A	ENSP00000502738.1:n.363G>A
ENST00000674775.1:n.398G>A
ENST00000674955.1:c.1198G>A	ENSP00000502463.1:p.Asp400Asn
ENST00000675118.1:c.686G>A
ENST00000675305.1:c.518G>A	ENSP00000502365.1:n.518G>A
ENST00000675310.1:n.138G>A
ENST00000675493.1:n.359G>A
ENST00000675615.1:c.1198G>A	ENSP00000502413.1:p.Asp400Asn
ENST00000675648.1:n.573G>A
ENST00000675684.1:c.325G>A	ENSP00000502192.1:p.Asp109Asn
ENST00000675755.1:n.138G>A
ENST00000676083.1:n.138G>A
ENST00000676173.1:n.1242G>A
ENST00000676228.1:c.*521G>A	ENSP00000502375.1:n.*521G>A
ENST00000676240.1:n.138G>A
ENST00000676400.1:n.138G>A
ENST00000255078.7:c.1198G>A	ENSP00000255078.3:p.Asp400Asn
ENST00000568742.1:n.308G>A
NM_002180.2:c.1198G>A , LRG_250t1:c.1198G>A	NP_002171.2:p.Asp400Asn
XM_005273974.2:c.187G>A	XP_005274031.1:p.Asp63Asn
XM_005273976.1:c.1198G>A	XP_005274033.1:p.Asp400Asn
XR_247198.1:n.1300G>A
XR_949903.1:n.1300G>A
XM_005273976.2:c.1198G>A	XP_005274033.1:p.Asp400Asn
XM_017017669.2:c.187G>A	XP_016873158.1:p.Asp63Asn
XM_017017670.2:c.187G>A	XP_016873159.1:p.Asp63Asn
XM_017017671.2:c.1198G>A	XP_016873160.1:p.Asp400Asn
XR_949903.3:n.1296G>A
NM_002180.3:c.1198G>A MANE Select	NP_002171.2:p.Asp400Asn