Canonical Allele Identifier: CA475204503

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1241285720
• MyVariant Identifiers: chr11:g.68704423A>G (hg19) ; chr11:g.68936955A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936955A>G , CM000673.2:g.68936955A>G	GRCh38
NC_000011.9:g.68704423A>G , CM000673.1:g.68704423A>G	GRCh37
NC_000011.8:g.68460999A>G	NCBI36
NG_007976.1:g.38105A>G , LRG_250:g.38105A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2475A>G MANE Select	ENSP00000255078.4:p.Pro825=
ENST00000674675.1:c.620A>G
ENST00000674878.1:c.580A>G
ENST00000675118.1:c.1963A>G
ENST00000675389.1:n.750A>G
ENST00000675615.1:c.2475A>G	ENSP00000502413.1:p.Pro825=
ENST00000675648.1:n.1850A>G
ENST00000675916.1:c.719A>G
ENST00000676173.1:n.3220A>G
ENST00000676182.1:c.906A>G
ENST00000676228.1:c.*1798A>G	ENSP00000502375.1:n.*1798A>G
ENST00000255078.7:c.2475A>G	ENSP00000255078.3:p.Pro825=
ENST00000539064.5:n.2234A>G
ENST00000543739.5:n.1468A>G
NM_002180.2:c.2475A>G , LRG_250t1:c.2475A>G	NP_002171.2:p.Pro825=
XM_005273974.2:c.1464A>G	XP_005274031.1:p.Pro488=
XM_005273975.2:c.1347A>G	XP_005274032.1:p.Pro449=
XM_011544994.1:c.1242A>G	XP_011543296.1:p.Pro414=
XR_949903.1:n.2577A>G
XM_005273975.3:c.1347A>G	XP_005274032.1:p.Pro449=
XM_017017669.2:c.1464A>G	XP_016873158.1:p.Pro488=
XM_017017670.2:c.1464A>G	XP_016873159.1:p.Pro488=
XR_949903.3:n.2573A>G
NM_002180.3:c.2475A>G MANE Select	NP_002171.2:p.Pro825=