Canonical Allele Identifier: CA381651570

Gene: IGHMBP2

Linked Data

• dbSNP Id: rs1594455433
• MyVariant Identifiers: chr11:g.68703752A>C (hg19) ; chr11:g.68936284A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936284A>C , CM000673.2:g.68936284A>C	GRCh38
NC_000011.9:g.68703752A>C , CM000673.1:g.68703752A>C	GRCh37
NC_000011.8:g.68460328A>C	NCBI36
NG_007976.1:g.37434A>C , LRG_250:g.37434A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.1804A>C MANE Select	ENSP00000255078.4:p.Thr602Pro
ENST00000674675.1:c.48A>C
ENST00000674878.1:c.48A>C
ENST00000674955.1:c.*521A>C	ENSP00000502463.1:n.*521A>C
ENST00000675118.1:c.1292A>C
ENST00000675389.1:n.79A>C
ENST00000675615.1:c.1804A>C	ENSP00000502413.1:p.Thr602Pro
ENST00000675648.1:n.1179A>C
ENST00000675916.1:c.48A>C
ENST00000676173.1:n.2549A>C
ENST00000676182.1:c.235A>C
ENST00000676228.1:c.*1127A>C	ENSP00000502375.1:n.*1127A>C
ENST00000255078.7:c.1804A>C	ENSP00000255078.3:p.Thr602Pro
ENST00000539064.5:n.1563A>C
ENST00000541229.5:n.499A>C
ENST00000543739.5:n.797A>C
ENST00000545475.1:n.400A>C
NM_002180.2:c.1804A>C , LRG_250t1:c.1804A>C	NP_002171.2:p.Thr602Pro
XM_005273974.2:c.793A>C	XP_005274031.1:p.Thr265Pro
XM_005273975.2:c.676A>C	XP_005274032.1:p.Thr226Pro
XM_011544994.1:c.571A>C	XP_011543296.1:p.Thr191Pro
XR_949903.1:n.1906A>C
XM_005273975.3:c.676A>C	XP_005274032.1:p.Thr226Pro
XM_017017669.2:c.793A>C	XP_016873158.1:p.Thr265Pro
XM_017017670.2:c.793A>C	XP_016873159.1:p.Thr265Pro
XR_949903.3:n.1902A>C
NM_002180.3:c.1804A>C MANE Select	NP_002171.2:p.Thr602Pro