Canonical Allele Identifier: CA679634350

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1292380105
• gnomAD v4: 11-68934198-C-G
• MyVariant Identifiers: chr11:g.68701666C>G (hg19) ; chr11:g.68934198C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68934198C>G , CM000673.2:g.68934198C>G	GRCh38
NC_000011.9:g.68701666C>G , CM000673.1:g.68701666C>G	GRCh37
NC_000011.8:g.68458242C>G	NCBI36
NG_007976.1:g.35348C>G , LRG_250:g.35348C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1538-266C>G MANE Select	ENSP00000255078.4:n.1538-266C>G
ENST00000674955.1:c.*255-266C>G	ENSP00000502463.1:n.*255-266C>G
ENST00000675118.1:c.1026-266C>G
ENST00000675205.1:n.184-266C>G
ENST00000675615.1:c.1538-266C>G	ENSP00000502413.1:n.1538-266C>G
ENST00000675648.1:n.913-266C>G
ENST00000675997.1:n.113-266C>G
ENST00000676173.1:n.2283-266C>G
ENST00000676228.1:c.*861-266C>G	ENSP00000502375.1:n.*861-266C>G
ENST00000255078.7:c.1538-266C>G	ENSP00000255078.3:n.1538-266C>G
ENST00000539064.5:n.1297-266C>G
ENST00000541229.5:n.233-266C>G
ENST00000543739.5:n.655-266C>G
NM_002180.2:c.1538-266C>G , LRG_250t1:c.1538-266C>G	NP_002171.2:n.1538-266C>G
XM_005273974.2:c.527-266C>G	XP_005274031.1:n.527-266C>G
XM_005273975.2:c.410-266C>G	XP_005274032.1:n.410-266C>G
XM_011544994.1:c.305-266C>G	XP_011543296.1:n.305-266C>G
XR_949903.1:n.1640-266C>G
XM_005273975.3:c.410-266C>G	XP_005274032.1:n.410-266C>G
XM_017017669.2:c.527-266C>G	XP_016873158.1:n.527-266C>G
XM_017017670.2:c.527-266C>G	XP_016873159.1:n.527-266C>G
XM_017017671.2:c.1538-266C>G	XP_016873160.1:n.1538-266C>G
XR_949903.3:n.1636-266C>G
NM_002180.3:c.1538-266C>G MANE Select	NP_002171.2:n.1538-266C>G