Canonical Allele Identifier: CA381652972

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs2154008870
• MyVariant Identifiers: chr11:g.68704127G>T (hg19) ; chr11:g.68936659G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936659G>T , CM000673.2:g.68936659G>T	GRCh38
NC_000011.9:g.68704127G>T , CM000673.1:g.68704127G>T	GRCh37
NC_000011.8:g.68460703G>T	NCBI36
NG_007976.1:g.37809G>T , LRG_250:g.37809G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2179G>T MANE Select	ENSP00000255078.4:p.Asp727Tyr
ENST00000674675.1:c.423G>T
ENST00000674878.1:c.423G>T
ENST00000674955.1:c.*896G>T	ENSP00000502463.1:n.*896G>T
ENST00000675118.1:c.1667G>T
ENST00000675389.1:n.454G>T
ENST00000675615.1:c.2179G>T	ENSP00000502413.1:p.Asp727Tyr
ENST00000675648.1:n.1554G>T
ENST00000675916.1:c.423G>T
ENST00000676173.1:n.2924G>T
ENST00000676182.1:c.610G>T
ENST00000676228.1:c.*1502G>T	ENSP00000502375.1:n.*1502G>T
ENST00000255078.7:c.2179G>T	ENSP00000255078.3:p.Asp727Tyr
ENST00000539064.5:n.1938G>T
ENST00000543739.5:n.1172G>T
NM_002180.2:c.2179G>T , LRG_250t1:c.2179G>T	NP_002171.2:p.Asp727Tyr
XM_005273974.2:c.1168G>T	XP_005274031.1:p.Asp390Tyr
XM_005273975.2:c.1051G>T	XP_005274032.1:p.Asp351Tyr
XM_011544994.1:c.946G>T	XP_011543296.1:p.Asp316Tyr
XR_949903.1:n.2281G>T
XM_005273975.3:c.1051G>T	XP_005274032.1:p.Asp351Tyr
XM_017017669.2:c.1168G>T	XP_016873158.1:p.Asp390Tyr
XM_017017670.2:c.1168G>T	XP_016873159.1:p.Asp390Tyr
XR_949903.3:n.2277G>T
NM_002180.3:c.2179G>T MANE Select	NP_002171.2:p.Asp727Tyr