Canonical Allele Identifier: CA381653016

Gene: IGHMBP2

Linked Data

• gnomAD v4: 11-68936680-G-C
• MyVariant Identifiers: chr11:g.68704148G>C (hg19) ; chr11:g.68936680G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936680G>C , CM000673.2:g.68936680G>C	GRCh38
NC_000011.9:g.68704148G>C , CM000673.1:g.68704148G>C	GRCh37
NC_000011.8:g.68460724G>C	NCBI36
NG_007976.1:g.37830G>C , LRG_250:g.37830G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2200G>C MANE Select	ENSP00000255078.4:p.Val734Leu
ENST00000674675.1:c.444G>C
ENST00000674878.1:c.444G>C
ENST00000674955.1:c.*917G>C	ENSP00000502463.1:n.*917G>C
ENST00000675118.1:c.1688G>C
ENST00000675389.1:n.475G>C
ENST00000675615.1:c.2200G>C	ENSP00000502413.1:p.Val734Leu
ENST00000675648.1:n.1575G>C
ENST00000675916.1:c.444G>C
ENST00000676173.1:n.2945G>C
ENST00000676182.1:c.631G>C
ENST00000676228.1:c.*1523G>C	ENSP00000502375.1:n.*1523G>C
ENST00000255078.7:c.2200G>C	ENSP00000255078.3:p.Val734Leu
ENST00000539064.5:n.1959G>C
ENST00000543739.5:n.1193G>C
NM_002180.2:c.2200G>C , LRG_250t1:c.2200G>C	NP_002171.2:p.Val734Leu
XM_005273974.2:c.1189G>C	XP_005274031.1:p.Val397Leu
XM_005273975.2:c.1072G>C	XP_005274032.1:p.Val358Leu
XM_011544994.1:c.967G>C	XP_011543296.1:p.Val323Leu
XR_949903.1:n.2302G>C
XM_005273975.3:c.1072G>C	XP_005274032.1:p.Val358Leu
XM_017017669.2:c.1189G>C	XP_016873158.1:p.Val397Leu
XM_017017670.2:c.1189G>C	XP_016873159.1:p.Val397Leu
XR_949903.3:n.2298G>C
NM_002180.3:c.2200G>C MANE Select	NP_002171.2:p.Val734Leu