Canonical Allele Identifier: CA381644219

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68682291G>T (hg19) ; chr11:g.68914823G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914823G>T , CM000673.2:g.68914823G>T	GRCh38
NC_000011.9:g.68682291G>T , CM000673.1:g.68682291G>T	GRCh37
NC_000011.8:g.68438867G>T	NCBI36
NG_007976.1:g.15973G>T , LRG_250:g.15973G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.712G>T MANE Select	ENSP00000255078.4:p.Val238Phe
ENST00000539224.2:c.841G>T
ENST00000674955.1:c.712G>T	ENSP00000502463.1:p.Val238Phe
ENST00000675118.1:c.59G>T
ENST00000675119.1:c.1G>T	ENSP00000501861.1:p.Val1Phe
ENST00000675305.1:c.1G>T	ENSP00000502365.1:p.Val1Phe
ENST00000675464.1:c.1G>T	ENSP00000502650.1:p.Val1Phe
ENST00000675615.1:c.712G>T	ENSP00000502413.1:p.Val238Phe
ENST00000675683.1:c.99G>T
ENST00000676173.1:n.756G>T
ENST00000676228.1:c.*35G>T	ENSP00000502375.1:n.*35G>T
ENST00000676239.1:n.26G>T
ENST00000255078.7:c.712G>T	ENSP00000255078.3:p.Val238Phe
ENST00000539224.1:c.*35G>T	ENSP00000440465.1:n.*35G>T
NM_002180.2:c.712G>T , LRG_250t1:c.712G>T	NP_002171.2:p.Val238Phe
XM_005273974.2:c.-300G>T	XP_005274031.1:n.-300G>T
XM_005273976.1:c.712G>T	XP_005274033.1:p.Val238Phe
XR_247198.1:n.814G>T
XR_949903.1:n.814G>T
XM_005273976.2:c.712G>T	XP_005274033.1:p.Val238Phe
XM_017017669.2:c.-300G>T	XP_016873158.1:n.-300G>T
XM_017017670.2:c.-300G>T	XP_016873159.1:n.-300G>T
XM_017017671.2:c.712G>T	XP_016873160.1:p.Val238Phe
XR_949903.3:n.810G>T
NM_002180.3:c.712G>T MANE Select	NP_002171.2:p.Val238Phe