Canonical Allele Identifier: CA381644382

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68682376G>C (hg19) ; chr11:g.68914908G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914908G>C , CM000673.2:g.68914908G>C	GRCh38
NC_000011.9:g.68682376G>C , CM000673.1:g.68682376G>C	GRCh37
NC_000011.8:g.68438952G>C	NCBI36
NG_007976.1:g.16058G>C , LRG_250:g.16058G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.797G>C MANE Select	ENSP00000255078.4:p.Gly266Ala
ENST00000539224.2:c.926G>C
ENST00000674955.1:c.797G>C	ENSP00000502463.1:p.Gly266Ala
ENST00000675118.1:c.144G>C
ENST00000675119.1:c.86G>C	ENSP00000501861.1:p.Gly29Ala
ENST00000675305.1:c.86G>C	ENSP00000502365.1:p.Gly29Ala
ENST00000675464.1:c.86G>C	ENSP00000502650.1:p.Gly29Ala
ENST00000675615.1:c.797G>C	ENSP00000502413.1:p.Gly266Ala
ENST00000675683.1:c.184G>C
ENST00000676173.1:n.841G>C
ENST00000676228.1:c.*120G>C	ENSP00000502375.1:n.*120G>C
ENST00000676239.1:n.111G>C
ENST00000255078.7:c.797G>C	ENSP00000255078.3:p.Gly266Ala
ENST00000539224.1:c.*120G>C	ENSP00000440465.1:n.*120G>C
NM_002180.2:c.797G>C , LRG_250t1:c.797G>C	NP_002171.2:p.Gly266Ala
XM_005273974.2:c.-215G>C	XP_005274031.1:n.-215G>C
XM_005273976.1:c.797G>C	XP_005274033.1:p.Gly266Ala
XR_247198.1:n.899G>C
XR_949903.1:n.899G>C
XM_005273976.2:c.797G>C	XP_005274033.1:p.Gly266Ala
XM_017017669.2:c.-215G>C	XP_016873158.1:n.-215G>C
XM_017017670.2:c.-215G>C	XP_016873159.1:n.-215G>C
XM_017017671.2:c.797G>C	XP_016873160.1:p.Gly266Ala
XR_949903.3:n.895G>C
NM_002180.3:c.797G>C MANE Select	NP_002171.2:p.Gly266Ala