Canonical Allele Identifier: CA2724579313
Gene: IGHMBP2 HGNC NCBI

Linked Data

dbSNP Id: rs2154008636

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68933768T>G , CM000673.2:g.68933768T>G GRCh38
NC_000011.9:g.68701236T>G , CM000673.1:g.68701236T>G GRCh37
NC_000011.8:g.68457812T>G NCBI36
NG_007976.1:g.34918T>G , LRG_250:g.34918T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000255078.8:c.1419-27T>G MANE Select ENSP00000255078.4:n.1419-27T>G
ENST00000674955.1:c.*136-27T>G ENSP00000502463.1:n.*136-27T>G
ENST00000675118.1:c.907-27T>G
ENST00000675205.1:n.183+287T>G
ENST00000675615.1:c.1419-27T>G ENSP00000502413.1:n.1419-27T>G
ENST00000675648.1:n.794-27T>G
ENST00000675997.1:n.113-696T>G
ENST00000676173.1:n.2164-27T>G
ENST00000676228.1:c.*742-27T>G ENSP00000502375.1:n.*742-27T>G
ENST00000255078.7:c.1419-27T>G ENSP00000255078.3:n.1419-27T>G
ENST00000537458.5:n.536-27T>G
ENST00000539064.5:n.1178-27T>G
ENST00000541229.5:n.87T>G
ENST00000543739.5:n.536-27T>G
NM_002180.2:c.1419-27T>G , LRG_250t1:c.1419-27T>G NP_002171.2:n.1419-27T>G
XM_005273974.2:c.408-27T>G XP_005274031.1:n.408-27T>G
XM_005273975.2:c.291-27T>G XP_005274032.1:n.291-27T>G
XM_011544994.1:c.186-27T>G XP_011543296.1:n.186-27T>G
XR_949903.1:n.1521-27T>G
XM_005273975.3:c.291-27T>G XP_005274032.1:n.291-27T>G
XM_017017669.2:c.408-27T>G XP_016873158.1:n.408-27T>G
XM_017017670.2:c.408-27T>G XP_016873159.1:n.408-27T>G
XM_017017671.2:c.1419-27T>G XP_016873160.1:n.1419-27T>G
XR_949903.3:n.1517-27T>G
NM_002180.3:c.1419-27T>G MANE Select NP_002171.2:n.1419-27T>G