Canonical Allele Identifier: CA6153373

Gene: IGHMBP2

Linked Data

• ClinVar Variation Id: 2066295
• ClinVar RCV Id: RCV002949016
• dbSNP Id: rs750936839
• ExAC: 11:68682281 C / T
• gnomAD v2: 11-68682281-C-T
• gnomAD v3: 11-68914813-C-T
• gnomAD v4: 11-68914813-C-T
• MyVariant Identifiers: chr11:g.68682281C>T (hg19) ; chr11:g.68914813C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68914813C>T , CM000673.2:g.68914813C>T	GRCh38
NC_000011.9:g.68682281C>T , CM000673.1:g.68682281C>T	GRCh37
NC_000011.8:g.68438857C>T	NCBI36
NG_007976.1:g.15963C>T , LRG_250:g.15963C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.712-10C>T MANE Select	ENSP00000255078.4:n.712-10C>T
ENST00000539224.2:c.841-10C>T
ENST00000674955.1:c.712-10C>T	ENSP00000502463.1:n.712-10C>T
ENST00000675118.1:c.59-10C>T
ENST00000675615.1:c.712-10C>T	ENSP00000502413.1:n.712-10C>T
ENST00000675683.1:c.99-10C>T
ENST00000676173.1:n.756-10C>T
ENST00000676228.1:c.*35-10C>T	ENSP00000502375.1:n.*35-10C>T
ENST00000676239.1:n.26-10C>T
ENST00000255078.7:c.712-10C>T	ENSP00000255078.3:n.712-10C>T
ENST00000539224.1:c.*35-10C>T	ENSP00000440465.1:n.*35-10C>T
NM_002180.2:c.712-10C>T , LRG_250t1:c.712-10C>T	NP_002171.2:n.712-10C>T
XM_005273974.2:c.-300-10C>T	XP_005274031.1:n.-300-10C>T
XM_005273976.1:c.712-10C>T	XP_005274033.1:n.712-10C>T
XR_247198.1:n.814-10C>T
XR_949903.1:n.814-10C>T
XM_005273976.2:c.712-10C>T	XP_005274033.1:n.712-10C>T
XM_017017669.2:c.-300-10C>T	XP_016873158.1:n.-300-10C>T
XM_017017670.2:c.-300-10C>T	XP_016873159.1:n.-300-10C>T
XM_017017671.2:c.712-10C>T	XP_016873160.1:n.712-10C>T
XR_949903.3:n.810-10C>T
NM_002180.3:c.712-10C>T MANE Select	NP_002171.2:n.712-10C>T