Canonical Allele Identifier: CA381647971

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68929358G>T , CM000673.2:g.68929358G>T	GRCh38
NC_000011.9:g.68696826G>T , CM000673.1:g.68696826G>T	GRCh37
NC_000011.8:g.68453402G>T	NCBI36
NG_007976.1:g.30508G>T , LRG_250:g.30508G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002180.3:c.1235+1G>T MANE Select	NP_002171.2:n.1235+1G>T
ENST00000255078.8:c.1235+1G>T MANE Select	ENSP00000255078.4:n.1235+1G>T
NM_002180.2:c.1235+1G>T , LRG_250t1:c.1235+1G>T	NP_002171.2:n.1235+1G>T
ENST00000255078.7:c.1235+1G>T	ENSP00000255078.3:n.1235+1G>T
ENST00000568742.1:n.345+1G>T
ENST00000674698.1:n.175+1G>T
ENST00000674955.1:c.1235+1G>T	ENSP00000502463.1:n.1235+1G>T
ENST00000675118.1:c.723+1G>T
ENST00000675310.1:n.175+1G>T
ENST00000675615.1:c.1235+1G>T	ENSP00000502413.1:n.1235+1G>T
ENST00000675648.1:n.610+1G>T
ENST00000675755.1:n.175+1G>T
ENST00000676083.1:n.175+1G>T
ENST00000676173.1:n.1279+1G>T
ENST00000676228.1:c.*558+1G>T	ENSP00000502375.1:n.*558+1G>T
ENST00000676240.1:n.175+1G>T
ENST00000676400.1:n.175+1G>T
XM_005273974.2:c.224+1G>T	XP_005274031.1:n.224+1G>T
XM_005273976.1:c.1235+1G>T	XP_005274033.1:n.1235+1G>T
XM_005273976.2:c.1235+1G>T	XP_005274033.1:n.1235+1G>T
XM_017017669.2:c.224+1G>T	XP_016873158.1:n.224+1G>T
XM_017017670.2:c.224+1G>T	XP_016873159.1:n.224+1G>T
XM_017017671.2:c.1235+1G>T	XP_016873160.1:n.1235+1G>T
XR_247198.1:n.1337+1G>T
XR_949903.1:n.1337+1G>T
XR_949903.3:n.1333+1G>T