Canonical Allele Identifier: CA6153807

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs11600808
• ExAC: 11:68703864 C / T
• gnomAD v2: 11-68703864-C-T
• gnomAD v4: 11-68936396-C-T
• MyVariant Identifiers: chr11:g.68703864C>T (hg19) ; chr11:g.68936396C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936396C>T , CM000673.2:g.68936396C>T	GRCh38
NC_000011.9:g.68703864C>T , CM000673.1:g.68703864C>T	GRCh37
NC_000011.8:g.68460440C>T	NCBI36
NG_007976.1:g.37546C>T , LRG_250:g.37546C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1916C>T MANE Select	ENSP00000255078.4:p.Ala639Val
ENST00000674675.1:c.160C>T
ENST00000674878.1:c.160C>T
ENST00000674955.1:c.*633C>T	ENSP00000502463.1:n.*633C>T
ENST00000675118.1:c.1404C>T
ENST00000675389.1:n.191C>T
ENST00000675615.1:c.1916C>T	ENSP00000502413.1:p.Ala639Val
ENST00000675648.1:n.1291C>T
ENST00000675916.1:c.160C>T
ENST00000676173.1:n.2661C>T
ENST00000676182.1:c.347C>T
ENST00000676228.1:c.*1239C>T	ENSP00000502375.1:n.*1239C>T
ENST00000255078.7:c.1916C>T	ENSP00000255078.3:p.Ala639Val
ENST00000539064.5:n.1675C>T
ENST00000543739.5:n.909C>T
ENST00000545475.1:n.512C>T
NM_002180.2:c.1916C>T , LRG_250t1:c.1916C>T	NP_002171.2:p.Ala639Val
XM_005273974.2:c.905C>T	XP_005274031.1:p.Ala302Val
XM_005273975.2:c.788C>T	XP_005274032.1:p.Ala263Val
XM_011544994.1:c.683C>T	XP_011543296.1:p.Ala228Val
XR_949903.1:n.2018C>T
XM_005273975.3:c.788C>T	XP_005274032.1:p.Ala263Val
XM_017017669.2:c.905C>T	XP_016873158.1:p.Ala302Val
XM_017017670.2:c.905C>T	XP_016873159.1:p.Ala302Val
XR_949903.3:n.2014C>T
NM_002180.3:c.1916C>T MANE Select	NP_002171.2:p.Ala639Val