Canonical Allele Identifier: CA475186416

Gene: IGHMBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68908239C>T , CM000673.2:g.68908239C>T	GRCh38
NC_000011.9:g.68675707C>T , CM000673.1:g.68675707C>T	GRCh37
NC_000011.8:g.68432283C>T	NCBI36
NG_007976.1:g.9389C>T , LRG_250:g.9389C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002180.3:c.351C>T MANE Select	NP_002171.2:p.Ala117=
ENST00000255078.8:c.351C>T MANE Select	ENSP00000255078.4:p.Ala117=
NM_002180.2:c.351C>T , LRG_250t1:c.351C>T	NP_002171.2:p.Ala117=
ENST00000255078.7:c.351C>T	ENSP00000255078.3:p.Ala117=
ENST00000539224.1:c.351C>T	ENSP00000440465.1:p.Ala117=
ENST00000539224.2:c.314C>T
ENST00000544541.1:c.*91C>T	ENSP00000443343.1:n.*91C>T
ENST00000674583.1:c.314C>T
ENST00000674597.1:c.162C>T
ENST00000674955.1:c.351C>T	ENSP00000502463.1:p.Ala117=
ENST00000675142.1:n.314C>T
ENST00000675469.1:c.227C>T
ENST00000675615.1:c.351C>T	ENSP00000502413.1:p.Ala117=
ENST00000675674.1:n.314C>T
ENST00000675873.1:c.314C>T
ENST00000676173.1:n.395C>T
ENST00000676228.1:c.351C>T	ENSP00000502375.1:p.Ala117=
XM_005273974.2:c.-661C>T	XP_005274031.1:n.-661C>T
XM_005273976.1:c.351C>T	XP_005274033.1:p.Ala117=
XM_005273976.2:c.351C>T	XP_005274033.1:p.Ala117=
XM_017017669.2:c.-563C>T	XP_016873158.1:n.-563C>T
XM_017017671.2:c.351C>T	XP_016873160.1:p.Ala117=
XR_247198.1:n.453C>T
XR_949903.1:n.453C>T
XR_949903.3:n.449C>T