Canonical Allele Identifier: CA2574904180

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68915099T>A , CM000673.2:g.68915099T>A	GRCh38
NC_000011.9:g.68682567T>A , CM000673.1:g.68682567T>A	GRCh37
NC_000011.8:g.68439143T>A	NCBI36
NG_007976.1:g.16249T>A , LRG_250:g.16249T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.912+76T>A MANE Select	ENSP00000255078.4:n.912+76T>A
ENST00000539224.2:c.1041+76T>A
ENST00000674955.1:c.912+76T>A	ENSP00000502463.1:n.912+76T>A
ENST00000675118.1:c.259+76T>A
ENST00000675119.1:c.201+76T>A	ENSP00000501861.1:n.201+76T>A
ENST00000675305.1:c.201+76T>A	ENSP00000502365.1:n.201+76T>A
ENST00000675464.1:c.195+82T>A	ENSP00000502650.1:n.195+82T>A
ENST00000675615.1:c.912+76T>A	ENSP00000502413.1:n.912+76T>A
ENST00000675683.1:c.299+76T>A
ENST00000676173.1:n.956+76T>A
ENST00000676228.1:c.*235+76T>A	ENSP00000502375.1:n.*235+76T>A
ENST00000255078.7:c.912+76T>A	ENSP00000255078.3:n.912+76T>A
NM_002180.2:c.912+76T>A , LRG_250t1:c.912+76T>A	NP_002171.2:n.912+76T>A
XM_005273974.2:c.-100+76T>A	XP_005274031.1:n.-100+76T>A
XM_005273976.1:c.912+76T>A	XP_005274033.1:n.912+76T>A
XR_247198.1:n.1014+76T>A
XR_949903.1:n.1014+76T>A
XM_005273976.2:c.912+76T>A	XP_005274033.1:n.912+76T>A
XM_017017669.2:c.-100+76T>A	XP_016873158.1:n.-100+76T>A
XM_017017670.2:c.-100+76T>A	XP_016873159.1:n.-100+76T>A
XM_017017671.2:c.912+76T>A	XP_016873160.1:n.912+76T>A
XR_949903.3:n.1010+76T>A
NM_002180.3:c.912+76T>A MANE Select	NP_002171.2:n.912+76T>A