Canonical Allele Identifier: CA381653255

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704254A>C (hg19) ; chr11:g.68936786A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936786A>C , CM000673.2:g.68936786A>C	GRCh38
NC_000011.9:g.68704254A>C , CM000673.1:g.68704254A>C	GRCh37
NC_000011.8:g.68460830A>C	NCBI36
NG_007976.1:g.37936A>C , LRG_250:g.37936A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2306A>C MANE Select	ENSP00000255078.4:p.His769Pro
ENST00000674675.1:c.550A>C
ENST00000674878.1:c.547+3A>C
ENST00000674955.1:c.*1023A>C	ENSP00000502463.1:n.*1023A>C
ENST00000675118.1:c.1794A>C
ENST00000675389.1:n.581A>C
ENST00000675615.1:c.2306A>C	ENSP00000502413.1:p.His769Pro
ENST00000675648.1:n.1681A>C
ENST00000675916.1:c.550A>C
ENST00000676173.1:n.3051A>C
ENST00000676182.1:c.737A>C
ENST00000676228.1:c.*1629A>C	ENSP00000502375.1:n.*1629A>C
ENST00000255078.7:c.2306A>C	ENSP00000255078.3:p.His769Pro
ENST00000539064.5:n.2065A>C
ENST00000543739.5:n.1299A>C
NM_002180.2:c.2306A>C , LRG_250t1:c.2306A>C	NP_002171.2:p.His769Pro
XM_005273974.2:c.1295A>C	XP_005274031.1:p.His432Pro
XM_005273975.2:c.1178A>C	XP_005274032.1:p.His393Pro
XM_011544994.1:c.1073A>C	XP_011543296.1:p.His358Pro
XR_949903.1:n.2408A>C
XM_005273975.3:c.1178A>C	XP_005274032.1:p.His393Pro
XM_017017669.2:c.1295A>C	XP_016873158.1:p.His432Pro
XM_017017670.2:c.1295A>C	XP_016873159.1:p.His432Pro
XR_949903.3:n.2404A>C
NM_002180.3:c.2306A>C MANE Select	NP_002171.2:p.His769Pro