Canonical Allele Identifier: CA475279436
Gene: IGHMBP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.68704036G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68936568G>A , CM000673.2:g.68936568G>A GRCh38
NC_000011.9:g.68704036G>A , CM000673.1:g.68704036G>A GRCh37
NC_000011.8:g.68460612G>A NCBI36
NG_007976.1:g.37718G>A , LRG_250:g.37718G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.2088G>A MANE Select ENSP00000255078.4:p.Lys696=
ENST00000674675.1:c.332G>A
ENST00000674878.1:c.332G>A
ENST00000674955.1:c.*805G>A ENSP00000502463.1:n.*805G>A
ENST00000675118.1:c.1576G>A
ENST00000675389.1:n.363G>A
ENST00000675615.1:c.2088G>A ENSP00000502413.1:p.Lys696=
ENST00000675648.1:n.1463G>A
ENST00000675916.1:c.332G>A
ENST00000676173.1:n.2833G>A
ENST00000676182.1:c.519G>A
ENST00000676228.1:c.*1411G>A ENSP00000502375.1:n.*1411G>A
ENST00000255078.7:c.2088G>A ENSP00000255078.3:p.Lys696=
ENST00000539064.5:n.1847G>A
ENST00000543739.5:n.1081G>A
NM_002180.2:c.2088G>A , LRG_250t1:c.2088G>A NP_002171.2:p.Lys696=
XM_005273974.2:c.1077G>A XP_005274031.1:p.Lys359=
XM_005273975.2:c.960G>A XP_005274032.1:p.Lys320=
XM_011544994.1:c.855G>A XP_011543296.1:p.Lys285=
XR_949903.1:n.2190G>A
XM_005273975.3:c.960G>A XP_005274032.1:p.Lys320=
XM_017017669.2:c.1077G>A XP_016873158.1:p.Lys359=
XM_017017670.2:c.1077G>A XP_016873159.1:p.Lys359=
XR_949903.3:n.2186G>A
NM_002180.3:c.2088G>A MANE Select NP_002171.2:p.Lys696=