Canonical Allele Identifier: CA475204391

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs139065967
• MyVariant Identifiers: chr11:g.68703862G>C (hg19) ; chr11:g.68936394G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936394G>C , CM000673.2:g.68936394G>C	GRCh38
NC_000011.9:g.68703862G>C , CM000673.1:g.68703862G>C	GRCh37
NC_000011.8:g.68460438G>C	NCBI36
NG_007976.1:g.37544G>C , LRG_250:g.37544G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1914G>C MANE Select	ENSP00000255078.4:p.Thr638=
ENST00000674675.1:c.158G>C
ENST00000674878.1:c.158G>C
ENST00000674955.1:c.*631G>C	ENSP00000502463.1:n.*631G>C
ENST00000675118.1:c.1402G>C
ENST00000675389.1:n.189G>C
ENST00000675615.1:c.1914G>C	ENSP00000502413.1:p.Thr638=
ENST00000675648.1:n.1289G>C
ENST00000675916.1:c.158G>C
ENST00000676173.1:n.2659G>C
ENST00000676182.1:c.345G>C
ENST00000676228.1:c.*1237G>C	ENSP00000502375.1:n.*1237G>C
ENST00000255078.7:c.1914G>C	ENSP00000255078.3:p.Thr638=
ENST00000539064.5:n.1673G>C
ENST00000543739.5:n.907G>C
ENST00000545475.1:n.510G>C
NM_002180.2:c.1914G>C , LRG_250t1:c.1914G>C	NP_002171.2:p.Thr638=
XM_005273974.2:c.903G>C	XP_005274031.1:p.Thr301=
XM_005273975.2:c.786G>C	XP_005274032.1:p.Thr262=
XM_011544994.1:c.681G>C	XP_011543296.1:p.Thr227=
XR_949903.1:n.2016G>C
XM_005273975.3:c.786G>C	XP_005274032.1:p.Thr262=
XM_017017669.2:c.903G>C	XP_016873158.1:p.Thr301=
XM_017017670.2:c.903G>C	XP_016873159.1:p.Thr301=
XR_949903.3:n.2012G>C
NM_002180.3:c.1914G>C MANE Select	NP_002171.2:p.Thr638=