Canonical Allele Identifier: CA381644539

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68682455T>G (hg19) ; chr11:g.68914987T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914987T>G , CM000673.2:g.68914987T>G	GRCh38
NC_000011.9:g.68682455T>G , CM000673.1:g.68682455T>G	GRCh37
NC_000011.8:g.68439031T>G	NCBI36
NG_007976.1:g.16137T>G , LRG_250:g.16137T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.876T>G MANE Select	ENSP00000255078.4:p.Ile292Met
ENST00000539224.2:c.1005T>G
ENST00000674955.1:c.876T>G	ENSP00000502463.1:p.Ile292Met
ENST00000675118.1:c.223T>G
ENST00000675119.1:c.165T>G	ENSP00000501861.1:p.Ile55Met
ENST00000675305.1:c.165T>G	ENSP00000502365.1:p.Ile55Met
ENST00000675464.1:c.165T>G	ENSP00000502650.1:p.Ile55Met
ENST00000675615.1:c.876T>G	ENSP00000502413.1:p.Ile292Met
ENST00000675683.1:c.263T>G
ENST00000676173.1:n.920T>G
ENST00000676228.1:c.*199T>G	ENSP00000502375.1:n.*199T>G
ENST00000676239.1:n.190T>G
ENST00000255078.7:c.876T>G	ENSP00000255078.3:p.Ile292Met
NM_002180.2:c.876T>G , LRG_250t1:c.876T>G	NP_002171.2:p.Ile292Met
XM_005273974.2:c.-136T>G	XP_005274031.1:n.-136T>G
XM_005273976.1:c.876T>G	XP_005274033.1:p.Ile292Met
XR_247198.1:n.978T>G
XR_949903.1:n.978T>G
XM_005273976.2:c.876T>G	XP_005274033.1:p.Ile292Met
XM_017017669.2:c.-136T>G	XP_016873158.1:n.-136T>G
XM_017017670.2:c.-136T>G	XP_016873159.1:n.-136T>G
XM_017017671.2:c.876T>G	XP_016873160.1:p.Ile292Met
XR_949903.3:n.974T>G
NM_002180.3:c.876T>G MANE Select	NP_002171.2:p.Ile292Met