Canonical Allele Identifier: CA381652667

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68703981A>C (hg19) ; chr11:g.68936513A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936513A>C , CM000673.2:g.68936513A>C	GRCh38
NC_000011.9:g.68703981A>C , CM000673.1:g.68703981A>C	GRCh37
NC_000011.8:g.68460557A>C	NCBI36
NG_007976.1:g.37663A>C , LRG_250:g.37663A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2033A>C MANE Select	ENSP00000255078.4:p.Gln678Pro
ENST00000674675.1:c.277A>C
ENST00000674878.1:c.277A>C
ENST00000674955.1:c.*750A>C	ENSP00000502463.1:n.*750A>C
ENST00000675118.1:c.1521A>C
ENST00000675389.1:n.308A>C
ENST00000675615.1:c.2033A>C	ENSP00000502413.1:p.Gln678Pro
ENST00000675648.1:n.1408A>C
ENST00000675916.1:c.277A>C
ENST00000676173.1:n.2778A>C
ENST00000676182.1:c.464A>C
ENST00000676228.1:c.*1356A>C	ENSP00000502375.1:n.*1356A>C
ENST00000255078.7:c.2033A>C	ENSP00000255078.3:p.Gln678Pro
ENST00000539064.5:n.1792A>C
ENST00000543739.5:n.1026A>C
NM_002180.2:c.2033A>C , LRG_250t1:c.2033A>C	NP_002171.2:p.Gln678Pro
XM_005273974.2:c.1022A>C	XP_005274031.1:p.Gln341Pro
XM_005273975.2:c.905A>C	XP_005274032.1:p.Gln302Pro
XM_011544994.1:c.800A>C	XP_011543296.1:p.Gln267Pro
XR_949903.1:n.2135A>C
XM_005273975.3:c.905A>C	XP_005274032.1:p.Gln302Pro
XM_017017669.2:c.1022A>C	XP_016873158.1:p.Gln341Pro
XM_017017670.2:c.1022A>C	XP_016873159.1:p.Gln341Pro
XR_949903.3:n.2131A>C
NM_002180.3:c.2033A>C MANE Select	NP_002171.2:p.Gln678Pro