Canonical Allele Identifier: CA381652052

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1388711726
• MyVariant Identifiers: chr11:g.68703882A>G (hg19) ; chr11:g.68936414A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936414A>G , CM000673.2:g.68936414A>G	GRCh38
NC_000011.9:g.68703882A>G , CM000673.1:g.68703882A>G	GRCh37
NC_000011.8:g.68460458A>G	NCBI36
NG_007976.1:g.37564A>G , LRG_250:g.37564A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1934A>G MANE Select	ENSP00000255078.4:p.Asp645Gly
ENST00000674675.1:c.178A>G
ENST00000674878.1:c.178A>G
ENST00000674955.1:c.*651A>G	ENSP00000502463.1:n.*651A>G
ENST00000675118.1:c.1422A>G
ENST00000675389.1:n.209A>G
ENST00000675615.1:c.1934A>G	ENSP00000502413.1:p.Asp645Gly
ENST00000675648.1:n.1309A>G
ENST00000675916.1:c.178A>G
ENST00000676173.1:n.2679A>G
ENST00000676182.1:c.365A>G
ENST00000676228.1:c.*1257A>G	ENSP00000502375.1:n.*1257A>G
ENST00000255078.7:c.1934A>G	ENSP00000255078.3:p.Asp645Gly
ENST00000539064.5:n.1693A>G
ENST00000543739.5:n.927A>G
ENST00000545475.1:n.530A>G
NM_002180.2:c.1934A>G , LRG_250t1:c.1934A>G	NP_002171.2:p.Asp645Gly
XM_005273974.2:c.923A>G	XP_005274031.1:p.Asp308Gly
XM_005273975.2:c.806A>G	XP_005274032.1:p.Asp269Gly
XM_011544994.1:c.701A>G	XP_011543296.1:p.Asp234Gly
XR_949903.1:n.2036A>G
XM_005273975.3:c.806A>G	XP_005274032.1:p.Asp269Gly
XM_017017669.2:c.923A>G	XP_016873158.1:p.Asp308Gly
XM_017017670.2:c.923A>G	XP_016873159.1:p.Asp308Gly
XR_949903.3:n.2032A>G
NM_002180.3:c.1934A>G MANE Select	NP_002171.2:p.Asp645Gly