Canonical Allele Identifier: CA381650373
Gene: IGHMBP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68933909C>A , CM000673.2:g.68933909C>A GRCh38
NC_000011.9:g.68701377C>A , CM000673.1:g.68701377C>A GRCh37
NC_000011.8:g.68457953C>A NCBI36
NG_007976.1:g.35059C>A , LRG_250:g.35059C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.1533C>A MANE Select ENSP00000255078.4:p.Asn511Lys
ENST00000674955.1:c.*250C>A ENSP00000502463.1:n.*250C>A
ENST00000675118.1:c.1021C>A
ENST00000675205.1:n.183+428C>A
ENST00000675615.1:c.1533C>A ENSP00000502413.1:p.Asn511Lys
ENST00000675648.1:n.908C>A
ENST00000675997.1:n.113-555C>A
ENST00000676173.1:n.2278C>A
ENST00000676228.1:c.*856C>A ENSP00000502375.1:n.*856C>A
ENST00000255078.7:c.1533C>A ENSP00000255078.3:p.Asn511Lys
ENST00000537458.5:n.650C>A
ENST00000539064.5:n.1292C>A
ENST00000541229.5:n.228C>A
ENST00000543739.5:n.650C>A
NM_002180.2:c.1533C>A , LRG_250t1:c.1533C>A NP_002171.2:p.Asn511Lys
XM_005273974.2:c.522C>A XP_005274031.1:p.Asn174Lys
XM_005273975.2:c.405C>A XP_005274032.1:p.Asn135Lys
XM_011544994.1:c.300C>A XP_011543296.1:p.Asn100Lys
XR_949903.1:n.1635C>A
XM_005273975.3:c.405C>A XP_005274032.1:p.Asn135Lys
XM_017017669.2:c.522C>A XP_016873158.1:p.Asn174Lys
XM_017017670.2:c.522C>A XP_016873159.1:p.Asn174Lys
XM_017017671.2:c.1533C>A XP_016873160.1:p.Asn511Lys
XR_949903.3:n.1631C>A
NM_002180.3:c.1533C>A MANE Select NP_002171.2:p.Asn511Lys