Canonical Allele Identifier: CA381653482

Gene: IGHMBP2

Linked Data

• MyVariant Identifiers: chr11:g.68704337G>T (hg19) ; chr11:g.68936869G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68936869G>T , CM000673.2:g.68936869G>T	GRCh38
NC_000011.9:g.68704337G>T , CM000673.1:g.68704337G>T	GRCh37
NC_000011.8:g.68460913G>T	NCBI36
NG_007976.1:g.38019G>T , LRG_250:g.38019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255078.8:c.2389G>T MANE Select	ENSP00000255078.4:p.Ala797Ser
ENST00000674675.1:c.587+46G>T
ENST00000674878.1:c.548-54G>T
ENST00000675118.1:c.1877G>T
ENST00000675389.1:n.664G>T
ENST00000675615.1:c.2389G>T	ENSP00000502413.1:p.Ala797Ser
ENST00000675648.1:n.1764G>T
ENST00000675916.1:c.633G>T
ENST00000676173.1:n.3134G>T
ENST00000676182.1:c.820G>T
ENST00000676228.1:c.*1712G>T	ENSP00000502375.1:n.*1712G>T
ENST00000255078.7:c.2389G>T	ENSP00000255078.3:p.Ala797Ser
ENST00000539064.5:n.2148G>T
ENST00000543739.5:n.1382G>T
NM_002180.2:c.2389G>T , LRG_250t1:c.2389G>T	NP_002171.2:p.Ala797Ser
XM_005273974.2:c.1378G>T	XP_005274031.1:p.Ala460Ser
XM_005273975.2:c.1261G>T	XP_005274032.1:p.Ala421Ser
XM_011544994.1:c.1156G>T	XP_011543296.1:p.Ala386Ser
XR_949903.1:n.2491G>T
XM_005273975.3:c.1261G>T	XP_005274032.1:p.Ala421Ser
XM_017017669.2:c.1378G>T	XP_016873158.1:p.Ala460Ser
XM_017017670.2:c.1378G>T	XP_016873159.1:p.Ala460Ser
XR_949903.3:n.2487G>T
NM_002180.3:c.2389G>T MANE Select	NP_002171.2:p.Ala797Ser