Canonical Allele Identifier: CA381652060

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1859529795
• gnomAD v4: 11-68936417-T-C
• MyVariant Identifiers: chr11:g.68703885T>C (hg19) ; chr11:g.68936417T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936417T>C , CM000673.2:g.68936417T>C	GRCh38
NC_000011.9:g.68703885T>C , CM000673.1:g.68703885T>C	GRCh37
NC_000011.8:g.68460461T>C	NCBI36
NG_007976.1:g.37567T>C , LRG_250:g.37567T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1937T>C MANE Select	ENSP00000255078.4:p.Ile646Thr
ENST00000674675.1:c.181T>C
ENST00000674878.1:c.181T>C
ENST00000674955.1:c.*654T>C	ENSP00000502463.1:n.*654T>C
ENST00000675118.1:c.1425T>C
ENST00000675389.1:n.212T>C
ENST00000675615.1:c.1937T>C	ENSP00000502413.1:p.Ile646Thr
ENST00000675648.1:n.1312T>C
ENST00000675916.1:c.181T>C
ENST00000676173.1:n.2682T>C
ENST00000676182.1:c.368T>C
ENST00000676228.1:c.*1260T>C	ENSP00000502375.1:n.*1260T>C
ENST00000255078.7:c.1937T>C	ENSP00000255078.3:p.Ile646Thr
ENST00000539064.5:n.1696T>C
ENST00000543739.5:n.930T>C
ENST00000545475.1:n.533T>C
NM_002180.2:c.1937T>C , LRG_250t1:c.1937T>C	NP_002171.2:p.Ile646Thr
XM_005273974.2:c.926T>C	XP_005274031.1:p.Ile309Thr
XM_005273975.2:c.809T>C	XP_005274032.1:p.Ile270Thr
XM_011544994.1:c.704T>C	XP_011543296.1:p.Ile235Thr
XR_949903.1:n.2039T>C
XM_005273975.3:c.809T>C	XP_005274032.1:p.Ile270Thr
XM_017017669.2:c.926T>C	XP_016873158.1:p.Ile309Thr
XM_017017670.2:c.926T>C	XP_016873159.1:p.Ile309Thr
XR_949903.3:n.2035T>C
NM_002180.3:c.1937T>C MANE Select	NP_002171.2:p.Ile646Thr