Canonical Allele Identifier: CA6153848

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs771844457
• ExAC: 11:68704121 G / T
• gnomAD v2: 11-68704121-G-T
• gnomAD v4: 11-68936653-G-T
• MyVariant Identifiers: chr11:g.68704121G>T (hg19) ; chr11:g.68936653G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936653G>T , CM000673.2:g.68936653G>T	GRCh38
NC_000011.9:g.68704121G>T , CM000673.1:g.68704121G>T	GRCh37
NC_000011.8:g.68460697G>T	NCBI36
NG_007976.1:g.37803G>T , LRG_250:g.37803G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000255078.8:c.2173G>T MANE Select	ENSP00000255078.4:p.Gly725Cys
ENST00000674675.1:c.417G>T
ENST00000674878.1:c.417G>T
ENST00000674955.1:c.*890G>T	ENSP00000502463.1:n.*890G>T
ENST00000675118.1:c.1661G>T
ENST00000675389.1:n.448G>T
ENST00000675615.1:c.2173G>T	ENSP00000502413.1:p.Gly725Cys
ENST00000675648.1:n.1548G>T
ENST00000675916.1:c.417G>T
ENST00000676173.1:n.2918G>T
ENST00000676182.1:c.604G>T
ENST00000676228.1:c.*1496G>T	ENSP00000502375.1:n.*1496G>T
ENST00000255078.7:c.2173G>T	ENSP00000255078.3:p.Gly725Cys
ENST00000539064.5:n.1932G>T
ENST00000543739.5:n.1166G>T
NM_002180.2:c.2173G>T , LRG_250t1:c.2173G>T	NP_002171.2:p.Gly725Cys
XM_005273974.2:c.1162G>T	XP_005274031.1:p.Gly388Cys
XM_005273975.2:c.1045G>T	XP_005274032.1:p.Gly349Cys
XM_011544994.1:c.940G>T	XP_011543296.1:p.Gly314Cys
XR_949903.1:n.2275G>T
XM_005273975.3:c.1045G>T	XP_005274032.1:p.Gly349Cys
XM_017017669.2:c.1162G>T	XP_016873158.1:p.Gly388Cys
XM_017017670.2:c.1162G>T	XP_016873159.1:p.Gly388Cys
XR_949903.3:n.2271G>T
NM_002180.3:c.2173G>T MANE Select	NP_002171.2:p.Gly725Cys