Canonical Allele Identifier: CA381653991

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704509A>C (hg19) ; chr11:g.68937041A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68937041A>C , CM000673.2:g.68937041A>C	GRCh38
NC_000011.9:g.68704509A>C , CM000673.1:g.68704509A>C	GRCh37
NC_000011.8:g.68461085A>C	NCBI36
NG_007976.1:g.38191A>C , LRG_250:g.38191A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2561A>C MANE Select	ENSP00000255078.4:p.Gln854Pro
ENST00000674675.1:c.706A>C
ENST00000674878.1:c.666A>C
ENST00000675118.1:c.2049A>C
ENST00000675389.1:n.836A>C
ENST00000675615.1:c.2561A>C	ENSP00000502413.1:p.Gln854Pro
ENST00000675648.1:n.1936A>C
ENST00000675916.1:c.805A>C
ENST00000676173.1:n.3306A>C
ENST00000676182.1:c.992A>C
ENST00000676228.1:c.*1884A>C	ENSP00000502375.1:n.*1884A>C
ENST00000255078.7:c.2561A>C	ENSP00000255078.3:p.Gln854Pro
ENST00000539064.5:n.2320A>C
ENST00000543739.5:n.1554A>C
NM_002180.2:c.2561A>C , LRG_250t1:c.2561A>C	NP_002171.2:p.Gln854Pro
XM_005273974.2:c.1550A>C	XP_005274031.1:p.Gln517Pro
XM_005273975.2:c.1433A>C	XP_005274032.1:p.Gln478Pro
XM_011544994.1:c.1328A>C	XP_011543296.1:p.Gln443Pro
XR_949903.1:n.2663A>C
XM_005273975.3:c.1433A>C	XP_005274032.1:p.Gln478Pro
XM_017017669.2:c.1550A>C	XP_016873158.1:p.Gln517Pro
XM_017017670.2:c.1550A>C	XP_016873159.1:p.Gln517Pro
XR_949903.3:n.2659A>C
NM_002180.3:c.2561A>C MANE Select	NP_002171.2:p.Gln854Pro