Canonical Allele Identifier: CA6154083

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68939749C>T , CM000673.2:g.68939749C>T	GRCh38
NC_000011.9:g.68707217C>T , CM000673.1:g.68707217C>T	GRCh37
NC_000011.8:g.68463793C>T	NCBI36
NG_007976.1:g.40899C>T , LRG_250:g.40899C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002180.3:c.*18C>T MANE Select	NP_002171.2:n.*18C>T
ENST00000255078.8:c.*18C>T MANE Select	ENSP00000255078.4:n.*18C>T
NM_002180.2:c.*18C>T , LRG_250t1:c.*18C>T	NP_002171.2:n.*18C>T
ENST00000255078.7:c.*18C>T	ENSP00000255078.3:n.*18C>T
ENST00000543739.5:n.1993C>T
ENST00000544521.1:n.831C>T
ENST00000675118.1:c.2488C>T
ENST00000675648.1:n.2562C>T
ENST00000675916.1:c.1431C>T
ENST00000676173.1:n.3745C>T
XM_005273974.2:c.*18C>T	XP_005274031.1:n.*18C>T
XM_005273975.2:c.*18C>T	XP_005274032.1:n.*18C>T
XM_005273975.3:c.*18C>T	XP_005274032.1:n.*18C>T
XM_011544994.1:c.*18C>T	XP_011543296.1:n.*18C>T
XM_017017669.2:c.*18C>T	XP_016873158.1:n.*18C>T
XM_017017670.2:c.*18C>T	XP_016873159.1:n.*18C>T
XR_949903.1:n.3289C>T
XR_949903.3:n.3285C>T